Difference between revisions of "Healthcare Technology"

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Specifications should be functional specifications and drawn up based on features available in at least a few brands of the device commonly available in South Africa.  Before making a selection the following may be considered:  
 
Specifications should be functional specifications and drawn up based on features available in at least a few brands of the device commonly available in South Africa.  Before making a selection the following may be considered:  
  
* demonstration of devices by supplier;
+
*demonstration of devices by supplier;
* trial use of the device in a facility;
+
*trial use of the device in a facility;
* visit to a facility where the device is available;
+
*visit to a facility where the device is available;
* verbal presentation on device made by a supplier of the device; and
+
*verbal presentation on device made by a supplier of the device; and
* communication with existing users of the device both locally and abroad.
+
*communication with existing users of the device both locally and abroad.
  
 
A suggested format for specifications is as follows:
 
A suggested format for specifications is as follows:
  
* name of equipment;
+
*name of equipment;
* Function;
+
*Function;
* essential features;
+
*essential features;
* essential components;
+
*essential components;
* additional components;
+
*additional components;
* power supply;
+
*power supply;
* additional requirements; and
+
*additional requirements; and
* training – user training, maintenance training.
+
*training – user training, maintenance training.
  
 
In order to eliminate the possibility of outdated specifications being used, all specifications should have a validity date on the document. Specifications that are not valid or have expired should not be used. Copies of the latest specifications should be obtained from the appropriate HTM unit.
 
In order to eliminate the possibility of outdated specifications being used, all specifications should have a validity date on the document. Specifications that are not valid or have expired should not be used. Copies of the latest specifications should be obtained from the appropriate HTM unit.
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A sample specification (that for an infant incubator) is given in '''Annex I'''. For some equipment, such as sophisticated or imported items, or equipment which is new in the system, it may be necessary to specify the following item lines:
 
A sample specification (that for an infant incubator) is given in '''Annex I'''. For some equipment, such as sophisticated or imported items, or equipment which is new in the system, it may be necessary to specify the following item lines:
  
* '''Site preparation details''' – supplier should provide technical instructions and details so that this work can be planned, either in-house or by contracting out.
+
*'''Site preparation details''' – supplier should provide technical instructions and details so that this work can be planned, either in-house or by contracting out.
* '''Installation''' – assistance may be needed.
+
*'''Installation''' – assistance may be needed.
* '''Commissioning''' – assistance may again be required.
+
*'''Commissioning''' – assistance may again be required.
* '''Acceptance''' – the responsibilities of both the purchaser and supplier with respect to testing and/or acceptance of the goods must be clearly detailed.
+
*'''Acceptance''' – the responsibilities of both the purchaser and supplier with respect to testing and/or acceptance of the goods must be clearly detailed.
* '''Training''' of '''both''' users and technicians – help must be obtained if required.
+
*'''Training''' of '''both''' users and technicians – help must be obtained if required.
* '''Maintenance contract''' (an important part of after-sales support) – help must be requested if it is required. It will be necessary to agree and stipulate the duration<ins>,</ins> and whether it should extend beyond the warranty period, the cost and whether it includes the price of labour and spare parts, and the responsibilities of the owner and supplier.
+
*'''Maintenance contract''' (an important part of after-sales support) – help must be requested if it is required. It will be necessary to agree and stipulate the duration<ins>,</ins> and whether it should extend beyond the warranty period, the cost and whether it includes the price of labour and spare parts, and the responsibilities of the owner and supplier.
  
 
There are a number of technical and environmental factors that need to be taken into account. For example:
 
There are a number of technical and environmental factors that need to be taken into account. For example:
  
* If the area has an unstable power supply, is the supplier able to offer technical solutions (such as voltage stabilisers, <ins>an </ins>uninterruptible power supply)?
+
*If the area has an unstable power supply, is the supplier able to offer technical solutions (such as voltage stabilisers, <ins>an </ins>uninterruptible power supply)?
* Will the geographical location (such as height above sea-level) affect the operation of equipment (such as motors, pressure vessels)? If so, can the manufacturer adjust the item<ins>’s</ins> specific needs?
+
*Will the geographical location (such as height above sea-level) affect the operation of equipment (such as motors, pressure vessels)? If so, can the manufacturer adjust the item<ins>’s</ins> specific needs?
* Extremes of temperature, humidity, and dust may adversely affect equipment operation, and may require solutions such as air-conditioning, silica gel, polymerised coatings for printed circuit boards, and filters.
+
*Extremes of temperature, humidity, and dust may adversely affect equipment operation, and may require solutions such as air-conditioning, silica gel, polymerised coatings for printed circuit boards, and filters.
  
 
This information can be included within the generic equipment specifications. However, since much of the information is common to many pieces of equipment, some health service providers have found it simpler to develop a separate summary ''Technical and Environmental Data Sheet'', which can be referred to in the purchase documents. This data sheet can be distributed to all suppliers, interested parties, trade delegations and other relevant bodies. Such a data sheet can be provided regardless of the length of specification or the procurement method used, ensuring that all parties are kept informed of prevailing national conditions which could affect the operation of equipment.  
 
This information can be included within the generic equipment specifications. However, since much of the information is common to many pieces of equipment, some health service providers have found it simpler to develop a separate summary ''Technical and Environmental Data Sheet'', which can be referred to in the purchase documents. This data sheet can be distributed to all suppliers, interested parties, trade delegations and other relevant bodies. Such a data sheet can be provided regardless of the length of specification or the procurement method used, ensuring that all parties are kept informed of prevailing national conditions which could affect the operation of equipment.  
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The following details should be included in a Technical and Environmental Data Sheet:  
 
The following details should be included in a Technical and Environmental Data Sheet:  
  
* Electricity supply – mains or other supply, voltage and frequency values and fluctuations.  
+
*Electricity supply – mains or other supply, voltage and frequency values and fluctuations.
* Water supply – mains or other supply, quality and pressure.  
+
*Water supply – mains or other supply, quality and pressure.
* Environment: height above sea-level; mean temperature and fluctuations; humidity; dust level; vermin problems, etc.  
+
*Environment: height above sea-level; mean temperature and fluctuations; humidity; dust level; vermin problems, etc.
* Manufacturing quality – international or local standards required.  
+
*Manufacturing quality – international or local standards required.
* Language required – main and secondary.  
+
*Language required – main and secondary.
* Technology level required – manual, electro-mechanical or micro-processor controlled.  
+
*Technology level required – manual, electro-mechanical or micro-processor controlled.
  
=== Evaluation and comparison process ===
+
===Evaluation and comparison process===
 
The process of evaluation and comparison can often be time consuming. However, it is important to ensure that decisions for awarding contracts are not made simply on the basis of which items are the cheapest. During evaluation the items should be assessed against the requirements specified in the purchase document. The most common way to evaluate offers is to use an elimination process, where some offers are rejected at each stage. Offers should be judged against the following criteria:
 
The process of evaluation and comparison can often be time consuming. However, it is important to ensure that decisions for awarding contracts are not made simply on the basis of which items are the cheapest. During evaluation the items should be assessed against the requirements specified in the purchase document. The most common way to evaluate offers is to use an elimination process, where some offers are rejected at each stage. Offers should be judged against the following criteria:
  
·       Compliance with requirements in the purchase document.
+
* Compliance with requirements in the purchase document.
 
+
* Technical nature of the offer (part of the product selection criteria).
·       Technical nature of the offer (part of the product selection criteria).
+
* Financial nature of the offer (part of the product selection criteria).
 
+
* Supplier qualification criteria.
·       Financial nature of the offer (part of the product selection criteria).
 
 
 
·       Supplier qualification criteria.
 
  
  
 
By doing this, decisions are based on best value for money for the whole life-cycle cost, rather than simply being based on the item’s purchase price.
 
By doing this, decisions are based on best value for money for the whole life-cycle cost, rather than simply being based on the item’s purchase price.
 
  
 
The process of evaluation and comparison must be fair and thorough. To achieve this, the process must follow a defined pattern to ensure all bids/quotes are dealt with in exactly the same way.
 
The process of evaluation and comparison must be fair and thorough. To achieve this, the process must follow a defined pattern to ensure all bids/quotes are dealt with in exactly the same way.
 
  
 
The evaluation process for tenders is similar to that for quotes, although the tender process is normally a far more comprehensive task and is also regulated by law. The tools for evaluation can be the same, but the amount of information required is usually much less with quotation methods. Obviously, if only three quotes are requested for a simple small order, the evaluation process should not take much time. The following evaluation steps are used, and some bids/quotes are rejected at the end of each step.
 
The evaluation process for tenders is similar to that for quotes, although the tender process is normally a far more comprehensive task and is also regulated by law. The tools for evaluation can be the same, but the amount of information required is usually much less with quotation methods. Obviously, if only three quotes are requested for a simple small order, the evaluation process should not take much time. The following evaluation steps are used, and some bids/quotes are rejected at the end of each step.
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'''Step 1: Checking for compliance'''
 
'''Step 1: Checking for compliance'''
 
  
 
The first step when evaluating offers is to determine which, if any, are not compliant with the technical, commercial, and other specifications in the purchase document. The procurement unit should be able to do this. It involves a more detailed examination of the offer to determine the compliance by the bidder with the requirements specified in the purchase document. This is known in tender processes as the '''substantial responsiveness''' of the bid. This process is more formal and comprehensive for tenders than for quotations.  
 
The first step when evaluating offers is to determine which, if any, are not compliant with the technical, commercial, and other specifications in the purchase document. The procurement unit should be able to do this. It involves a more detailed examination of the offer to determine the compliance by the bidder with the requirements specified in the purchase document. This is known in tender processes as the '''substantial responsiveness''' of the bid. This process is more formal and comprehensive for tenders than for quotations.  
 
  
 
A substantially responsive bid is one which:
 
A substantially responsive bid is one which:
  
·       conforms to all the terms and conditions; this means that the supplier has responded to all parts of the schedule of requirements, has filled in all the boxes, and is able to supply all the parts required; and
+
* conforms to all the terms and conditions; this means that the supplier has responded to all parts of the schedule of requirements, has filled in all the boxes, and is able to supply all the parts required; and
 
+
* also establishes the bidder’s qualifications to supply and deliver the products within the delivery schedule; for example, the supplier:
·       also establishes the bidder’s qualifications to supply and deliver the products within the delivery schedule; for example, the supplier:
 
  
 
- has enclosed signed audited accounts, signed company declarations on health, safety, and environmental activities, certificates of quality manufacturing, and a letter of authorisation from the manufacturer, and
 
- has enclosed signed audited accounts, signed company declarations on health, safety, and environmental activities, certificates of quality manufacturing, and a letter of authorisation from the manufacturer, and
  
 
- has nominated a representative in the country (if this was one of the compliance criteria).
 
- has nominated a representative in the country (if this was one of the compliance criteria).
 
  
 
All non-substantial bids will be rejected as non-responsive and should be excluded from further in-depth evaluation.
 
All non-substantial bids will be rejected as non-responsive and should be excluded from further in-depth evaluation.
 
  
 
In practice it is found that most bids contain reservations from one or more of the detailed requirements. If these are just minor adjustments and do not represent a substantial deviation from expressed interests, one can still conclude that the bid is substantially responsive and therefore should be included. However, the reservations for closer clarification should be listed.
 
In practice it is found that most bids contain reservations from one or more of the detailed requirements. If these are just minor adjustments and do not represent a substantial deviation from expressed interests, one can still conclude that the bid is substantially responsive and therefore should be included. However, the reservations for closer clarification should be listed.
 
  
 
To assist in this examination one could ask for other clarifications from the bidder. One may also wish to inspect the quality methods and production methods stated in their documents. This request and response should be in writing. The bidders, however, are not allowed to make any changes to the substance or price of their offers. After evaluating the offers for compliance, some offers are discarded as the suppliers fail. The remaining offers can go forward to be compared in terms of technical performance (Step 3).
 
To assist in this examination one could ask for other clarifications from the bidder. One may also wish to inspect the quality methods and production methods stated in their documents. This request and response should be in writing. The bidders, however, are not allowed to make any changes to the substance or price of their offers. After evaluating the offers for compliance, some offers are discarded as the suppliers fail. The remaining offers can go forward to be compared in terms of technical performance (Step 3).
 
  
 
'''Step 2: Preparing the evaluation information'''
 
'''Step 2: Preparing the evaluation information'''
 
  
 
The procurement unit should collate and compile the information from all the responsive bids into evaluation information sheets. '''''Box 10''''' gives an example of the sort of data that needs to be included.  
 
The procurement unit should collate and compile the information from all the responsive bids into evaluation information sheets. '''''Box 10''''' gives an example of the sort of data that needs to be included.  
 
  
 
Box 10: '''Evaluation information sheets'''
 
Box 10: '''Evaluation information sheets'''
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''Technical  product data:''
 
''Technical  product data:''
  
·        The  international/regional standards that the equipment adheres to.
+
* The  international/regional standards that the equipment adheres to.
 
+
* Whether the  operational method used is new, well tried, or old.
·        Whether the  operational method used is new, well tried, or old.
+
* The level of  sophistication of the technology and the operating technique.
 
+
* Which functions and  measurements do not meet the specifications in the purchase document.
·        The level of  sophistication of the technology and the operating technique.
+
* Whether any quality  assurance certificates apply to the equipment.
 
 
·        Which functions and  measurements do not meet the specifications in the purchase document.
 
 
 
·        Whether any quality  assurance certificates apply to the equipment.
 
  
 
''Accessories,  consumables, spare parts:''
 
''Accessories,  consumables, spare parts:''
  
·        A list and the cost of  accessories included in the offer.
+
* A list and the cost of  accessories included in the offer.
 
+
* A list and the cost of  consumables included in the offer.
·        A list and the cost of  consumables included in the offer.
+
* A list and the cost of  spare parts included in the offer.
 
+
* The length of time  spare parts will be available and their location.
·        A list and the cost of  spare parts included in the offer.
 
 
 
·        The length of time  spare parts will be available and their location.
 
  
 
''After-sales  service:''
 
''After-sales  service:''
  
·        Cost of after-sales  support.
+
* Cost of after-sales  support.
 
+
* Guarantee/warranty  periods.
·        Guarantee/warranty  periods.
+
* The details of the  after-sales support that can be provided.
 
 
·        The details of the  after-sales support that can be provided.
 
  
 
''Price  information:''
 
''Price  information:''
  
·        The price.
+
* The price.
 
+
* Delivery arrangements
·        Delivery arrangements
+
* Costs to install,  commission, and train.
 
+
* The life-cycle costs.
·        Costs to install,  commission, and train.
 
 
 
·        The life-cycle costs.
 
 
 
  
 
Note:  this is an example and not a comprehensive list. The information chosen to  include will depend upon the complexity of the equipment purchased – less  technical detail is needed for simple equipment or recurrent supplies.
 
Note:  this is an example and not a comprehensive list. The information chosen to  include will depend upon the complexity of the equipment purchased – less  technical detail is needed for simple equipment or recurrent supplies.
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Ideally the evaluation information sheets should allow side-by-side comparison of the offers. For tenders there are more responses and the orders tend to be more complex, so more paperwork is required to obtain a true comparison. Usually there is too much information to be compiled in a single sheet, so it may be better to use:  
 
Ideally the evaluation information sheets should allow side-by-side comparison of the offers. For tenders there are more responses and the orders tend to be more complex, so more paperwork is required to obtain a true comparison. Usually there is too much information to be compiled in a single sheet, so it may be better to use:  
  
·       one sheet for collating purely technical information about the product;
+
* one sheet for collating purely technical information about the product;
 
+
* one for information on accessories, consumables, and spare parts;
·       one for information on accessories, consumables, and spare parts;
+
* one for after-sales service; and
 
+
* one for price information.
·       one for after-sales service; and
 
 
 
·       one for price information.
 
 
 
  
 
The procurement unit should present the evaluation information sheets to the procurement/tender committee (for tenders and high-value quotes) or the Procurement Manager (for low-value quotes). They should be accompanied by an explanation of the requirements, main objectives, and any binding constraints. Then the technical evaluation process (Step 3) can commence.
 
The procurement unit should present the evaluation information sheets to the procurement/tender committee (for tenders and high-value quotes) or the Procurement Manager (for low-value quotes). They should be accompanied by an explanation of the requirements, main objectives, and any binding constraints. Then the technical evaluation process (Step 3) can commence.
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'''Step 3: Carrying out the technical evaluation'''
 
'''Step 3: Carrying out the technical evaluation'''
 
  
 
The procurement/tender committee should base its decision on advice from members of the group with professional knowledge relevant to the offer. If appropriate, it should also seek advice from representatives from the relevant user department and HTM team (for low-value quotes, the Procurement Manager should also seek advice from these end-users).
 
The procurement/tender committee should base its decision on advice from members of the group with professional knowledge relevant to the offer. If appropriate, it should also seek advice from representatives from the relevant user department and HTM team (for low-value quotes, the Procurement Manager should also seek advice from these end-users).
 
  
 
The committee should consider the product selection criteria, as set out in the purchase document. It is essential that the information provided by the supplier is related only to the equipment specification and the selection criteria listed in the purchase document – any additional information intended to sway the evaluation can be seen as corruption; hence the importance of detailing requirements adequately in the purchase document. The better the purchase document, the easier the evaluation process will be. '''''Box 11''''' lists a few points to remember, relating to the technical aspects of the offer.  
 
The committee should consider the product selection criteria, as set out in the purchase document. It is essential that the information provided by the supplier is related only to the equipment specification and the selection criteria listed in the purchase document – any additional information intended to sway the evaluation can be seen as corruption; hence the importance of detailing requirements adequately in the purchase document. The better the purchase document, the easier the evaluation process will be. '''''Box 11''''' lists a few points to remember, relating to the technical aspects of the offer.  
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Box 11: '''Summary technical assessment'''
 
Box 11: '''Summary technical assessment'''
 
{| class="wikitable"
 
{| class="wikitable"
|·        If a detailed  specification was issued, then every detail of the offer must be closely  checked to make sure it conforms to the original specification.
+
|
 
+
* If a detailed  specification was issued, then every detail of the offer must be closely  checked to make sure it conforms to the original specification.
·        If only a  brief specification was issued, then the checks should be limited to ensuring  the equipment or service offered meets the requirements.
+
* If only a  brief specification was issued, then the checks should be limited to ensuring  the equipment or service offered meets the requirements.
 
+
* Any  modifications or alternatives offered must be assessed individually, and  decisions made whether any one is more cost-effective than another.
·        Any  modifications or alternatives offered must be assessed individually, and  decisions made whether any one is more cost-effective than another.
+
* The technical  assessment includes suitability, safety, ability to commission and train,  after-sales support, warranty arrangements and more – do not simply assess  technical data concerning the equipment.
 
 
·        The technical  assessment includes suitability, safety, ability to commission and train,  after-sales support, warranty arrangements and more – do not simply assess  technical data concerning the equipment.
 
 
|}  
 
|}  
  
 
For both quotations and tenders it may be necessary to ask the supplier to clarify any ambiguities or uncertainties. Alternatively, a shortlist of suppliers can be drawn up and those included can be asked to demonstrate their equipment, as part of the technical evaluation (this is unlikely to be necessary for very simple equipment, and may be impossible for many overseas suppliers).
 
For both quotations and tenders it may be necessary to ask the supplier to clarify any ambiguities or uncertainties. Alternatively, a shortlist of suppliers can be drawn up and those included can be asked to demonstrate their equipment, as part of the technical evaluation (this is unlikely to be necessary for very simple equipment, and may be impossible for many overseas suppliers).
 
  
 
After the technical evaluation, some offers are discarded if they fail to meet the requirements. The remaining offers can go forward to be compared in terms of financial performance.
 
After the technical evaluation, some offers are discarded if they fail to meet the requirements. The remaining offers can go forward to be compared in terms of financial performance.
 
  
  
 
{{Expand}}
 
{{Expand}}
 
[[Category:Crosscutting Issues]]
 
[[Category:Crosscutting Issues]]

Revision as of 15:14, 30 September 2020

Background

Health technology context

Health Technology covers a wide range of apparatus, consumables, devices, equipment and instruments that would require many volumes of documents to cover effectively. This document, as part of the broader IUSS Norms and Standards project, aims to look at the key elements of Health Technology and its management as it manifests in healthcare facilities. The document specifically aims at framing the subject of Health Technology within the infrastructure development and operations domain.

The various definitions of Health Technology are listed in the Glossary but it is important to note that this document focuses on durable medical equipment and related consumables used in healthcare facilities. Hospital plant and machinery, normally associated with the building and most often installed as part of the building, are dealt with in various other documents in the IUSS document bouquet, either under the respective hospital engineering disciplines or under the respective clinical service area.

Application of the Guidelines

This document, published under the Health Facility guides, would be useful for practitioners of Health Technology Management both at the level of an individual facility and for groups of facilities (for example, in a district) and at any level of care. It would also be of great value for HTM practitioners and facility managers in general who might lack the first-hand experience of this relatively specialised field. In many cases the guidelines show the way towards developing specific and applicable solutions rather than being prescriptive. This approach is necessary to ensure that they remain sufficiently generic to be applied across a broad spectrum of scenarios. The document would also be of interest to health infrastructure professionals who might need specific insight into the domain of Health Technology and its management, recognising that technology and infrastructure are closely inter-related and will become ever more so in future healthcare systems.

Associated process and related documents

This document should be considered in the context of the solid platform provided by the Health Technology Policy and the Health Facilities Planning Directorates of the National Department of Health. This includes the Framework for Health Technology Policies which outlines the vision of a National Health Technology System; the draft Health Technology Management Policy document which inter alia outlines the organisational and structural requirements at all levels of governance pertaining to such a system; the Health Technology Strategy which outlines specific objectives and activities, with associated timeframes, for establishing a National Health Technology System; the Report of the Interim Steering Committee on Health Technology Assessment, which underlines the importance of having formal processes in place to assess issues of health technology cost-effectiveness, access, service-fit and social impact, amongst other “evaluative dimensions”; and lastly the draft Medical Device Regulations and associated background documents which – in their final form – will be promulgated under the South African Health Products Regulatory Agency (SAHPRA) Act .

Life cycle of Health Technology

Planning

Introduction

Planning and budgeting are often considered jointly since planning – for it to be effective – needs to take place within the context of policy, financial, and other constraints. Box 1 shows the overall process.

BOX 1: The planning and budgeting process (start-up)

Steps People responsible Actions
Plan and budget within the framework of guidance and direction from the national level. Health service managers at national level in consultation with managers at other levels. Framework requirements
  • follow regulations and standards set by government;
  • develop a Healthcare Technology Policy including decisions on standardisation, maintenance provision, finances for HTM activities, and the organisational structure for an HTM service;
  • define the overall “Vision” for healthcare delivery at each level of the health service;
  • develop “Standard Equipment Lists” which define the essential equipment stock for the healthcare to be delivered at each level;
  • use “Generic Equipment cifications” for acquisition ofequipment;
  • develop good policies for purchasing, donations, replacement, and disposal of equipment; and participate in the planning, equipping and operation of health facilities.
Increase the availability of planning skills for equipment at all service levels, by developing planning “tools” through one-off exercises. HTM working groups and sub-groups.



Finance officers.

Knowing where one is starting from
  • establish an Equipment Inventory to keep up-to-date records of the current equipment stock;
  • estimate the equipment stock values;
  • define the usage rates of equipment-related consumable items so that realistic estimates can be made of the finances required for equipment accessories, consumables, and spare parts; and
  • set up budget lines to record and monitor expenditure on all the different equipment activities.
Health management teams.



HTM working groups and sub-groups.

Knowing where one is headed
  • develop a library of literature and resources which will help with equipment planning and budgeting;
  • adapt the vision for healthcare delivery at their service level;
  • adopt good policies for purchasing, donations, replacement, and disposal of equipment;
  • adapt the Standard Equipment List for their service level;
  • develop generic equipment specifications and technical and environmental data; and estimate human resource requirements and associated “acquisition” and capacity building.
Ensure realistic estimates are made for all equipment-related allocations at all service.levels, by using budgeting “tools” to calculate expenditures required. HTM working groups and sub-groups.


HTM managers and their teams.

Capital budget calculations
  • calculate expenditure requirements for replacement items;
  • calculate expenditure requirements for new purchases;
  • calculate expenditure requirements for support activities linked to purchases and donations;
  • calculate expenditure requirements for pre-installation work; and
  • calculate expenditure requirements for major rehabilitation work.
Ensure realistic estimates are made for all equipment-related allocations at all service levels, by using budgeting “tools” to calculate expenditures required.

HTM managers and their teams.

Heads of section.


HTM working groups and sub-groups.

Recurrent budget calculations
  • calculate recurrent expenditure requirements for maintenance;
  • calculate recurrent expenditure requirements for consumable operating costs;
  • calculate recurrent expenditure requirements for administrative expenses; and
  • calculate recurrent expenditure requirements for ongoing training.
Use the tools to make long-term plans and budgets


HTM working groups and sub-groups.

Long-term planning
  • establish an Equipment Development Plan covering the priorities for equipment needs across their service level over time;
  • establish an Equipment Training Plan to cover the ongoing rolling programme of training required in relation to equipment activities;
  • establish a Core Equipment Expenditure Plan which prioritises equipment spending across the facility over the long term; and
  • establish a Core Equipment Financing Plan indicating possible sources of funds and related options.
Review the plans and budgets annually, and monitor progress in order to improve planning and budgeting.


HTM teams.

HTM working groups

and sub-groups.

Annual planning
  • update the Equipment Inventory;
  • update the Equipment Development Plan;
  • update the Equipment Training Plan;
  • cost the capital and recurrent requirements for the current year, and update the Core Equipment Expenditure Plan and Core Equipment Financing Plan; and
  • prioritise across their service level to obtain the annual purchase activities, annual rehabilitation activities, annual corrective activities, annual training activities, and thus the annual equipment budget.
Review the plans and budgets annually, and monitor progress in order to improve planning and budgeting.


HTM working groups.

Heads of department and HTM managers.


Health management

teams.

Monitoring progress
  • ensure annual plans are implemented;
  • study the implications arising from planning and budgeting;
  • request help for any deviations from plans such as emergency purchases, maintenance and consumable contingencies;
  • monitor actual expenditure against allocations;
  • seek the funding identified;
  • consider linking allocation of budgets to whether departments achieve their performance targets;
  • monitor progress through establishing planning and budgeting tools and associated indicators; and
  • ensure that the information generated is used to improve stock control, training, procurement, utilisation, etc.

Service and related technology planning

For healthcare technology to be managed effectively, a clear idea of healthcare delivery goals and targets is needed, as well as the context in which the technology is operating. Equipment should not be viewed in isolation – it is there for a purpose, and must be managed according to set objectives. For effective planning, access to a wide range of information and reference materials is needed, as well as a clear vision of the direction in which the health service is headed, plus identification of what equipment is required to help achieve the health service goals.

To inform the technology part of the debate, the HTM working group (at each level) should consider the equipment implications of the healthcare interventions suggested, and then offer technical advice to their health management team. Box 2 and Checklist 1 show some of the issues that the national, province/district- and facility level HTM working groups, respectively, should consider.

BOX 2: Baseline information on medical devices

Medical device situation Considerations Result
  • Availability and condition of medical devices (including type, number, location and physical condition).
  • Status of electrical, water, and waste disposal systems related to medical device use.
  • Medical equipment inventory including status and condition.
  • Current health technology management infrastructure (or lack thereof).
  • Facility map.
  • Medical equipment inventory (quantitative and qualitative).
  • Outline of health technology management infrastructure.


CHECKLIST 1: Equipment considerations for vision at national level

Issues Example
What expansion of services is necessary or feasible?
  • What should be the role of a hospital (central, referral, district) in terms of the interventions and procedures to be carried out? What does this mean in terms of equipment availability?
  • What type of care can be offered by rural, district or town health centres? Can any types of care be transferred over to them? What does this mean in terms of equipment availability?
  • It may be best to locate certain specialised services (such as intensive-care units) only at certain hospitals. Some specialised services, such as radiotherapy, may only ever be offered at national level. With pressures to reduce costs, improve efficiencies, and possibly to reduce staff numbers, can service provision be rationalised? Is expansion based only on needs that can be realistically met?
What are the implications in terms of staff, skills, resources, patient referral networks?
  • Introducing a new service has knock-on implications for human, material and financial resources. For example, should eye instruments be bought for a facility if there is no eye surgeon, or prospects of one becoming available? Or if the referral system is such that dialysis is only undertaken and supported at a central facility, one should think carefully before placing dialysis machines at other further locations. However, if such expanded “satellite” services are required, then all the resources required to ensure effective service provision should be identified, provided and maintained.
Are desired expansions financially affordable?
  • Although many hospitals may ideally wish to have fluoroscopy facilities (for example), at a cost of approximately $500 000 per suite, is this a feature each hospital can necessarily invest in?
Do the services suggested fit into the overall health service in the country?
  • Is it possible to develop a vision which fits in with the other health service provider organisations?

Planning and budgeting when starting out

Box 3 shows the minimum requirements for a scenario for an HTM system in its infancy, where the initial focus is not on long-term forward planning, but concentration on planning and budgeting on a yearly basis. As the system matures, other elements for forward planning can be added.

Box 3: Minimum planning and budgeting requirements

Planning and budgeting element If just starting out
1. Equipment inventory

2. Stock value estimates

3. Budget lines for equipment expenditures.

4. Usage rates for equipment-related consumable items.

5. Reference materials.

6. Developing the vision of service delivery for each facility type.

7. Standard Equipment Lists.

8. Purchasing, donations, replacement, and disposal policies.

9. Generic equipment specifications and technical data.

10. Capital budget calculations.

11. Recurrent budget calculations.

12. Equipment development plan.

13. Equipment training plan.

14. Core equipment expenditure plan.

15. Core equipment financing plan.

16. Annual equipment planning and budgeting.

17. Monitoring progress.

1. Essential to have.

2. Useful to carry out this exercise later on when rough estimates needed for long-term forward planning.

3. This alteration to budget layout can be done later, but it will help with analysis.

4. Useful to do this exercise as it helps with calculation of specific (annual) estimates.

5. These can be developed over time.

6. Should have an understanding of this, even if full exercise not undertaken.

7. Initially, list of urgent equipment needs drawn up by departments can be used. Later on, Standard Equipment Lists obtained elsewhere can be used.

8. Essential to have.

9. Initially learn from others. Later, develop own.

10. Initially learn how to make specific (annual) estimates; only learn the rough estimation methods when undertaking long-term planning.

11. Initially learn how to make specific (annual) estimates. Only learn the rough estimation methods when undertaking long-term planning.

12.  Use the basic equipment development planning process only, and only apply it to the short term.

13. Develop a straightforward one for the short term

14. Initially only plan annually (see below).

15. Initially only plan annually (see below).

16. Create annual actions plans and an equipment budget showing income and expenditure.

17. Undertake the basic elements only – progress with annual plans and tools, coping with emergencies, providing feedback.

Needs assessment

Standard lists of equipment

Once the vision for the direction of health service delivery has been developed, the healthcare interventions and procedures to be offered will be known. Based on this information, the Essential Service Packages can be developed; these will translate the vision into:

  • human resource requirements, and training needs;
  • space requirements, and facility and service installation needs; and
  • equipment requirements.

The tool used in the process of defining what equipment is needed for each healthcare intervention is the Standard Equipment List. This is:

  • a list of equipment typically required for each healthcare intervention (such as a healthcare function, activity, or procedure). For example, health service providers might list all equipment required for eye-testing, delivering twins, undertaking fluoroscopic examinations, or for testing blood for malaria;
  • organised by activity space or room (such as reception area or treatment room), and by department;
  • developed for every different level of healthcare delivery (such as district, province) since the equipment needs will differ depending on the vision for each level;
  • usually made up of everything including furniture, fittings and fixtures, in order to be useful for planners, architects, engineers and purchasers, and
  • a tool which allows healthcare managers to establish if the Vision is economically viable.

The Standard Equipment List must reflect the level of technology of the equipment. It should describe only technology that the facility can sustain (in other words, equipment which can be operated and maintained by existing staff, and for which there are adequate resources for its use). For example a department could have:

  • an electric suction pump or a foot-operated one;
  • a hydraulic operating table or an electrically controlled one;
  • a computerised laundry system or electro-mechanical machines; and
  • disposable syringes or re-usable/sterilisable ones.

It is important that any equipment suggested:

  • can fit into the rooms and space available. Reference should therefore be made to any building norms defining room sizes, flow patterns, and requirements for water, electricity, light levels and so on;
  • has the necessary utilities and associated plant (such as the power, water, waste management systems) available for it on each site - if such utilities are not available, it is pointless planning to invest in equipment which requires these utilities in order to work; and
  • can be operated and maintained by existing staff and skill levels, or for which the necessary training is available and affordable.

Usefulness of the standard equipment lists

A Standard Equipment List is an aid to the planning process. In order to plan what equipment to purchase, awareness of any shortfalls in equipment is needed. To determine such shortfalls, the Equipment Inventory needs to be compared with the Standard Equipment List. This will indicate whether any equipment is currently missing or needs to be purchased. Thus, the Standard Equipment List will assist in determining what equipment is:

  • necessary;
  • surplus;
  • extravagant; and
  • missing

in relation to the Vision for the service.

Responsibility for developing the Standard Equipment Lists varies from country to country. It is most important that this task is undertaken by a multidisciplinary team, so that decisions benefit from the skills and views of many disciplines, not just one or two. The health service planners at central/national level should consider developing Standard Equipment Lists in collaboration with staff from each level of the service, as indicated in Box 4 below.

Who/which level? Takes what action?
HTM working group at each level Organises special meetings of different types of staff to work on the Standard Equipment List. Then reports back to the Health Management Teams.
National level Takes the first step and runs specific exercises to establish the Standard Lists of Equipment for each clinical and support area, at each operational level.
Province/district level Takes the second step and adjusts the list on a regional/district basis to cover local variations.
Facility level Takes the third step and assesses:

- how they can provide the healthcare interventions; and

- what numbers of equipment they require depending on how they organise their work.

Organisational decisions influence the quantity of equipment. For example, the timing of clinics can reduce or increase the workload in the laboratory. Before ordering new equipment, its level of use will need to be assessed.

Equipment development plan

Especially for an HTM system that is not mature, it is essential to have important to have [BvR1] an equipment development plan; one suggestion for the development planning process is presented in Flowchart 1 below.

Flowchart 1: The basic equipment development planning process

Prioritising and appraisal of options

It is equally important, in the context of needs assessment, to critically examine the process and its outputs and outcomes. Checklist 2 below poses some key questions for consideration by the appropriate stakeholder/s.

Checklist 2: Key questions for prioritising and appraisal of options

Impact
  • Which changes would have the greatest positive impact in meeting needs?
  • Do the identified needs relate to a local or a national priority (e.g., maternal and child health, HIV/AIDS, etc.)?
  • What would be the implications of not addressing the needs?
Changeability
  • Which things can be changed and effectively improved?
  • What evidence is there of effective interventions?
  • Can negative impacts be stopped or reduced?
  • Are there national or local, professional or organisational policies that set out guidelines on what should be done (e.g. national frameworks, national guidance, etc.)?
Acceptability
  • Which of the options for change are likely to be most acceptable to the health service providers, to the target population, and to the managers?
  • What might be the “knock-on” effects, or unintended consequences, of making a change?
Resource feasibility
  • Which resources are required to implement the proposed changes?
  • Can existing resources be used differently?
  • Which resources will be released if ineffective actions are stopped/changed (e.g., proper management of health technology, etc.)?
  • Are there other resources available which have not been given prior consideration (e.g., income generation of laboratory services, consideration of public-private partnerships, assistance from NGOs, etc.)?
  • Which of the actions will achieve the greatest impact for the resources used?

Consumables

Consumables are a major contributor to equipment-related cost of ownership, and form a significant portion of recurrent and operational expenditure. It is therefore important to establish the consumables needs so that adequate provision is made and service delivery is not interrupted. Flowchart 2 below suggests a process to facilitate the needs assessment related to equipment-related consumables.

Asset management

Inventory

It is essential that an inventory (asset register) of medical equipment is maintained. However, it is both costly and time-consuming to include each and every medical device in an asset register. For those items in an asset register, the following information should be captured and verified:

  • Equipment type (an international nomenclature system such as the Universal Medical Device Nomenclature System (UMDNS) should be used so that all institutions use a common name for the same type of device).
  • Make/manufacturer.
  • Model.
  • Serial number.
  • Date of acquisition.
  • Price paid (include any costly accessories).
  • Supplier details (name, address, contact person, contact details).
  • Location – department or ward where the unit is used.

The responsibilities, activities and role-players relating to equipment inventory are shown in Box 5.


Box 5: Inventory-related responsibilities, activities and actors

Body Responsibility Activity People involved
HTM Service Creates and updates the Equipment Inventory. Organises the gathering of inventory data. Either by:
  • facility staff for their own facility;
  • district staff for the facilities in their district;
  • central staff for the health service as a whole; and
  • using specialist help.
Inventory team Visits each department in the health facility, and:
  • looks in all rooms, cupboards, etc.;
  • physically checks all equipment for the details required; and
  • fills in the Equipment Inventory Record Sheets.

If existing records are available:

  • modifies or expands the information as necessary to cover new items;
  • fills in any gaps;
  • corrects entries; andupdates data in order to make the Equipment Inventory as accurate as possible.
Due to the workload and knowledge required, it is useful for the team to be made up of:
  • two maintenance staff (from the relevant HTM team);
  • a senior equipment user from the facility; and
  • a member of staff from the department being assessed (who changes as team moves from department to department).
HTM teams Compile the Equipment Inventory.

Make hard copies.

  • Enter the data gathered, either onto an inventory card or a computer screen, for each individual device.
  • Create summaries, prepare and print out hard copies.
  • Provide a copy of the Equipment Inventory.to the Stores Controller for inclusion in the General Inventory held by stores.
Make use of trained technical staff and secretarial/computing support to assist with data entry.
Central-level HTM team Develops the Equipment Inventory as an active (regularly updated) resource. Analyses the Equipment Inventory for planning purposes.
  • Uses computer-based tools required for this purpose (for example, word-processing spreadsheets or specific commercial inventory products which staff have been trained on.
Makes use of support from staff trained in keeping computerised records.


Asset management system

Proper asset management requires an appropriate information system which can be used to maintain data on those items that have been included in the asset register.

Equipment audits provide a snapshot of equipment status in a facility or groups of facilities, and can be aggregated to reveal the situation at national level. Audit data also serves to inform decision making related to needs assessment, asset management, maintenance strategies, replacement planning, and so on.

Also, once an inventory system is up and running, it will be necessary to periodically obtain estimates of total equipment stock values – this is used, for example, in benchmarking the total expenditure on maintenance. Flowchart 3 below shows the process for obtain such estimates.

Asset management software

It is essential to adopt and standardise on an appropriate asset management information system. There are a number of such systems available; serious consideration should be given to open-source solutions and/or or solutions which are cost-effective and sustainable, requiring minimal support.

Budgeting & financing

Estimates of budget lines for equipment expenditure

It is essential to have budget lines for health technologies/medical equipment in national, province, district and facility budgets. A process for developing budget lines is shown in Box 6.


Box 6: Process for developing budget lines for equipment expenditure

People responsible Action
Finance officers, at all levels of the health service (central, province, district, facility) Establish different budget lines (sub-divisions) as itemised below:

a. capital funds to cover equipment replacement (depreciation);

b. capital funds to cover additional new equipment requirements;

c. capital funds to cover support activities which ensure equipment purchases can be used (installation, commissioning, and initial training);

d. capital funds to cover pre-installation work for equipment purchases;

e. capital funds to cover major rehabilitation projects;

f. recurrent funds to cover equipment maintenance costs, including spare parts, service contracts, and minor works;

g. recurrent funds to cover equipment operational costs, including consumable items and worn out accessories;

h. recurrent funds to cover equipment-related administration, including energy requirements; and

i. recurrent funds to cover ongoing training requirements.

HTM working groups Start using these budget lines to analyse how money is allocated and spent for equipment purposes.
Health service providers Ensure that budgets are presented by cost centre so that it is clear what allocations are made between national, provincial, district and facility levels. In this way, it can be seen what money is spent on equipment activities at each level of the health service. Lobby other bodies involved (such as Ministries of Finance, Public Works) to also show equipment expenditures to establish what is allocated by other agencies for equipment activities in the health service.


The high-level budgets thus obtained can then be “unpacked” into more detailed line expenditures, such as shown in Table 1 below, with projections covering 3-5-year budget cycles.

Estimates of maintenance costs for forward planning

An important – and often neglected – expenditure category is that of maintenance, be it for medical equipment or healthcare technologies and infrastructure in general. Box 7 unpacks the maintenance line item to indicate the various categories of maintenance-related expenditure for medical equipment, while Flowchart 4 suggests a process for estimating maintenance costs as part of planning.


Table 1: Example of a core equipment expenditure plan

Capital expenditure Short term Medium term
2012 2013 2014 2015
Replacement Use calculations for rough estimations (see Note below)
New equipment
Support activities linked to purchases
Pre-installation
Rehabilitation
Sub-total
Recurrent expenditure
Equipment maintenance Use calculations for rough estimations (see Note below)
Consumables
Administration
On-going training
Sub-total
Total expenditure

Note: Initially, rough estimates are used for the short- and long-term overview when preparing this Core Equipment Expenditure Plan. During annual planning the estimates are revised, using calculations for specific requirements, to obtain the Annual Equipment Budget. The experience gained from that annual revision process may mean that the long-term estimates in this Core Equipment Expenditure Plan may have to be altered, so that they are more realistic.


Box 7: Elements of annual maintenance budgets

I. Planned budgets:

These allocate funds for anticipated maintenance costs, which can be derived from the following main areas of expenditure:

a) spare parts – which are required regularly, determined from previous experience and any planned remedial work;

b) spare parts – which are required according to planned preventive maintenance (PPM) schedules and timetables;

c) maintenance materials – which are required regularly, determined by previous experience and any planned remedial work;

d) maintenance materials – which are required according to PPM schedules and timetables;

e) service contracts – required for any planned remedial work;

f) service contracts – for breakdowns which are likely to be required, determined from previous experience;

g) service contracts – required for PPM of complex equipment;

h) calibration of workshop test equipment;

i) replacement of tools at the end of their life;

j) office material; and

k) any increased maintenance requirements brought about by planned new equipment purchases under the capital expenditure budget.

Note: there will be other elements which may fall under other budgets. These could include:

  • other administrative costs which are included in budgets held by other departments;
  • major repair works – in some cases the planned rehabilitation of equipment which rquires major work with the purchase of substantial amounts of materials or contracts (the large sums of money required for such projects may have to fall under the capital budget); and
  • pre-installation work (such as site-preparation); this often falls under capital funds as it is linked to specific purchases.

II. Contingency budgets:

In addition to planned budgets, contingency budgets also exist. These allocate funds for unplanned maintenance work, such as emergencies, or sudden breakdowns which could not be predicted.


[See Section 10.2 for further discussion on maintenance-related issues].

Estimates of consumable operating costs for forward planning

In Section A2 (Needs assessment) the importance of consumables for proper functioning and utilisation was highlighted. Since medical devices cover such a wide spectrum, the related consumables require insight and good management. A number of alternative approaches are suggested:


i. Consumption depends on the type of equipment used, the service provided, and how many patients are seen. Therefore, a rough estimation of consumable operating costs can be obtained by evaluating past usage rates/expenditures, and comparing these with expected patient loads and specific equipment usage rates per intervention.

ii. If the equipment is part of a “closed” purchasing system, the consumables are only made by one manufacturer and one is limited to a single supplier; this monopoly often increases the consumable costs. If the equipment is part of an “open” purchasing system, anyone can supply the consumables and different manufacturers’ consumables could be used; this competition brings down costs of consumable. Costs can also be kept down by using items which can be sterilised/re-used.

iii. Consumable operating costs vary according to equipment type, and can be expressed as a percentage of purchase cost or stock value, as shown by the examples below. But as the majority of equipment is likely to be technology that has low to medium consumable costs, one could use averages of 3% of the stock value for equipment with low consumable usage rates, and for others as shown in Table 2.

Table 2: Rough estimates of consumables’ operating costs for forward planning

Description Consumable cost per year (relative to original purchase cost)
Equipment with high consumable operating costs, such as:
  • Haemodialysis machine
  • Automatic biochemical analyser
  • Automatic haematology analyser
  • Electrolyte analyser
  • Blood gas analyser
70-120%
Equipment with medium consumable operating costs, such as:
  • Conventional x-ray machine
  • Anaesthesia machine


30%

20%

  • ECG recorder, three-channel
  • Ultrasound, medical/obstetric
  • Ventilator, ICU
  • Physiological monitor
  • EEG machine
15-25%
  • Autoclave, steam
  • Incubator, baby, ICU
10-15%

5-15%

Equipment with low consumable operating costs, such as:
  • Centrifuge, electrical
  • Suction pump


5%

2-5%

  • Delivery bed
  • Operating theatre lamp
  • Slit lamp
  • Operating microscope
  • Water bath
1-2%


A different calculation is required when making specific or annual estimates. Annual operating budgets should be based on more exact estimates. These are not always easy to predict since epidemics, outbreaks, or surges in workload cannot, in most cases, be anticipated.

Generally with experience, and where standardisation of equipment is in place, the projection for equipment consumables and spare accessories becomes more predictable.

Specific or annual estimates of consumable operating costs

It is equally important to make provision for consumables on an annual basis. Flowchart 5 suggests how this could be done.

Estimates of equipment replacement costs

Equipment replacement needs to be provided for, especially in the case of complex and expensive equipment, to ensure that adequate resourcing is available at the appropriate time to ensure continuity – or at least minimal disruption – of service delivery. Flowchart 6 below suggests a process to establish estimates for replacement costs.

Rough estimates of equipment-related administrative costs for forward planning

The administrative costs associated with medical equipment are also seldom considered separately, since they are hidden within general overheads. Different countries suggest alternative approaches:


i. Administrative costs are a small percentage of any operating budget; for example:

  • the biggest percentage expense is for staff, taking 50-55%;
  • supplies/spares take 35-45%; and
  • administration takes only 10-20%.

Thus an equipment-user department could use an average of 15% of their its total operating budget for administrative costs.

ii. For HTM teams and clinical engineering service maintenance workshops, their administrative needs are not much higher than other administrative units in health facilities. Therefore, a reasonable estimate for the administrative costs[1] for HTM teams could be calculated by taking 10-20% of their total operating budget.

iii. A starting point is to use 5% of the equipment stock value to cover equipment-related administrative costs.

Requisitioning

The following checklists cover three commonly encountered scenarios:

Checklist 3: Request to purchase new equipment that is not yet in use at the institution

a. Why is it essential to have this equipment and how will it enhance the present patient care. How was this function performed before and up until this request?

b. Statistics of the patients who will be treated with this equipment.

c. Is this equipment in line with the norms of the service delivery – level of care –of the institution?

d. Accessibility to similar equipment or services in a close proximity to the Institution.

e.  Is suitable accommodation available to install the equipment (building and facilities). Is the structure suitable to carry the additional mass? This to be confirmed by the Engineering Services Manager, in writing.

f. Are there engineering services available to operate the equipment and has the availability of the service been confirmed in writing by the Engineering Services Manager, for instance:

  • sufficient water pressure and flow (hot and cold);
  • sufficient water pressure and flow (hot and cold);
  • medical gas and compressed air (at the correct pressures and flow);
  • sufficient power at the correct voltage and current levels;
  • if required, a UPS system with a sufficient capacity;
  • a power line-conditioning unit for sensitive electronic equipment;
  • if required (for example autoclaves), is steam, condensate return and drainage available; and
  • if required, is the ventilation and air-conditioning sufficient.

g. Are proper specifications available from the HTM unit or is suitable equipment available from an approved period tender?  State the tender and the item numbers.

h. Confirmation must be obtained from the Institution that they have a budget (sufficient funds) to pay for a service contract (where called for), as well as consumables and preventive and corrective maintenance of the new equipment.

i. Will not having the equipment in any way compromise patient care or safety?


Checklist 4: Request to replace existing equipment

a. Inventory of similar equipment available in the Institution.

b. Inventory of how many pieces of the type of equipment are functional.

c. Inventory of how many pieces of equipment are not functional and the reason thereof.

d. Is this equipment in line with the norms of service delivery – level of care – of the institution?

e. Reason for the condemning of the equipment, supported by a Condemning Certificate.

f. Where the replacement is a fixture for instance an x-ray machine or processor, what engineering or structural changes will be required?

g. Does the Institution have sufficient funds to purchase the equipment requested?

h. Does the Institution have a budget, sufficient funds to pay for a Comprehensive Service Contract for the equipment requested?

i. Is suitable accommodation available to install the equipment (building and facilities) and is the structure suitable to carry the additional mass? This to be confirmed by the Engineering Services Manager, in writing.

j. Are there engineering services available to operate the equipment and has the availability of the service been confirmed in writing by the Engineering Services Manager, for instance (as for above scenario – Checklist 5)?

k. Can this equipment be standardised for the reasons previously stated above?

l. Statistics of patients to be treated with the equipment requested.

m. Are there no other procedures available to treat the patients?

n. Will not having the equipment in any way compromise patient care or safety?

o.  Are there proper specifications from the Health Technology Unit available, or is suitable equipment available from an approved period tender?   State the tender and the item numbers.

Checklist 5: Request to purchase additional equipment similar to equipment already in use

a. Inventory of similar equipment available in the Institution.

b. Inventory of how many pieces of the type of equipment are functional.

c. Inventory of how many pieces of the type of equipment are not functional and the reason therefore.

d. Is this equipment in line with the norms of service delivery – level of care - of the institution?

e. Reason for requesting the additional equipment backed up with patient statistics.  Has the function or status of the Institution changed?

f. Does the institution have sufficient funds to purchase the equipment?

g. Does the institution have a budget, sufficient funds to pay for a comprehensive service contract for the equipment requested?

h. Can this equipment be standardised for the reasons previously stated?

i.  Are there no other procedures available to treat the patients?

j. Will not having the equipment in any way compromise patient care or safety? Are there proper specifications available from the Health Technology Unit or is suitable equipment available from an approved period tender.   State the tender and item numbers?

Procurement

Introduction

Procurement, from a healthcare service perspective, is probably the most important activity within the medical equipment life-cycle. If the right (competent) people are driving a transparent, criteria-driven (not interest-driven) process, it is likely that the healthcare system will avail itself of the technology that is most appropriate to the intended application, while addressing issues around effectiveness, cost-of-ownership, institutional fit, technology maturity and compatibility, user competence, maintenance and so on. In many countries, procurement is being placed in the hands of generic supply-chain management personnel with little specialised knowledge of medical equipment specifically, and health technologies in general. It is therefore essential to ensure that a supporting environment is created to minimise the possibility of sub-optimal procurement outcomes.


Procurement (for capital equipment as opposed to consumables) should be seen as a process with two phases: one that commences with planning and needs assessment and ends with commissioning, and the other that extends over its operational lifetime and ensures that the equipment is provided with the necessary accessories, consumables, maintenance support, and so on.


There are four reasons for procuring equipment, each of which provides a different goal which will dictate when to acquire equipment. These can be placed in the following order of priority (see Box 8 below). Within each of the four categories shown, priorities will have to be set, and these can be based on appropriate indicators.


Box 8: Example of valid reasons and order of priority for purchasing of equipment

1. To cover depreciation of equipment. Equipment is replaced as it reaches the end of its life and is taken out of service. This is necessary in order for the level of healthcare that is currently delivered to be sustained. [Note: This means that the size of the existing equipment stock remains the same, and does not imply an expansion of the health service.]
2. To obtain additional equipment items which are missing from the basic standard requirements. Additional equipment may be required in order to provide a basic standard level of care. [Note: Missing items are identified by comparing the Equipment Inventory with the Standard Equipment List for the facility.]
3. To obtain additional equipment items beyond the basic standard. This is done in order to upgrade the level of health service provided by the hospital. For example, new equipment may be needed to provide a new service, build a new special unit, or increase the level of care offered.
4. To obtain additional equipment items outside the facility’s own plans. This will only be applicable if the additional items have been called for by directives from the national or provincial ministry, and cannot be stopped/refused for political reasons, such as “out of the ordinary”, high profile, or political projects.


Of course, procurement is not a self-contained, isolated process but links up with many other equipment-related processes; these are shown in Box 9 below.

Planning tools How they help
When replacing items:
Replacement policy Establishing and implementing this tool is much more likely to ensure that the necessary regular planned replacement of equipment takes place.
Equipment inventory and maintenance record system These tools support identification of the need for replacement equipment at any time. For easy reference, estimated lifetimes for equipment could be entered into the inventory and could then prompt one when to purchase. The natural life of equipment is shortened by harsh environment, over-use, unskilled handling, neglect of maintenance and damage. Equipment malfunction and downtime also increase with the age of the equipment. Accordingly, cost-effectiveness decreases with age.
Replacement and condemnation criteria These assist with judging when equipment has reached the end of its life, and therefore with identifying when equipment needs replacing.
Core equipment expenditure plan Some of the equipment will have to be replaced every year, so it makes sense to spread budgeting for replacement over time. By allocating some money each year, one can avoid facing a large replacement bill later on. This tool should spread these costs over the long term. Equipment replacement needs can be estimated each year by assuming that each piece of equipment has an average lifetime of 10 years [1] - this means that on average 10% of equipment stock needs to be replaced each year.
Disposal policy and disposal procedures When equipment is replaced, these tools will assist with the disposal of the old device or system. There may be government regulations regarding disposal that will provide additional information.
Stock- control system Replacement equipment-related supplies should be purchased after an up-to-date stock take. Accurate stock control systems help with planning and ordering.
When buying additional new items:
Equipment development plan, and annual purchase plan New equipment should be purchased according to an annual purchase plan (drawn each year from a long-term equipment development plan). This is based on an up-to-date inventory and Standard Equipment List. Accurate inventory record-keeping helps with planning and ordering.
Package of inputs Planning in advance for what will be needed after the purchase is every bit as important as the purchase itself. Thus, one must ensure that the package of inputs required to keep equipment functioning through its life is procured.
Core equipment financing plan, and annual budget Capital expenditure can only take place once sufficient funding sources have been identified. The long-term Core Equipment Financing Plan and Annual Budget should allocate known and possible sources of funds against elements of planned expenditure.

Additional items of equipment may need to be procured to accompany/complement the original item, if it is to function properly in certain environments. For example:

  • a voltage stabiliser (surge suppressor plus filter) - this offers protection against power supply fluctuations, but does not protect against power cuts. It monitors the power supply, removes surges and spikes, and maintains a continuously regulated alternating current output to the item;
  • an uninterruptible power supply - this offers protection against blackouts and power cuts of limited duration;
  • an air-conditioning unit; and
  • a water filter or treatment plant.

Preparation of specifications

Specifications have to be drawn up for every device that is planned to be purchased. Standardised specifications need to be drawn up for commonly used devices which can then be modified (where necessary) at institutional level.

General terms and conditions should also be part of specifications, including stipulations like the local availability of essential spare parts, and the presence of a registered sole agent for the specific brand.


Specifications should be functional specifications and drawn up based on features available in at least a few brands of the device commonly available in South Africa.  Before making a selection the following may be considered:

  • demonstration of devices by supplier;
  • trial use of the device in a facility;
  • visit to a facility where the device is available;
  • verbal presentation on device made by a supplier of the device; and
  • communication with existing users of the device both locally and abroad.

A suggested format for specifications is as follows:

  • name of equipment;
  • Function;
  • essential features;
  • essential components;
  • additional components;
  • power supply;
  • additional requirements; and
  • training – user training, maintenance training.

In order to eliminate the possibility of outdated specifications being used, all specifications should have a validity date on the document. Specifications that are not valid or have expired should not be used. Copies of the latest specifications should be obtained from the appropriate HTM unit.

A sample specification (that for an infant incubator) is given in Annex I. For some equipment, such as sophisticated or imported items, or equipment which is new in the system, it may be necessary to specify the following item lines:

  • Site preparation details – supplier should provide technical instructions and details so that this work can be planned, either in-house or by contracting out.
  • Installation – assistance may be needed.
  • Commissioning – assistance may again be required.
  • Acceptance – the responsibilities of both the purchaser and supplier with respect to testing and/or acceptance of the goods must be clearly detailed.
  • Training of both users and technicians – help must be obtained if required.
  • Maintenance contract (an important part of after-sales support) – help must be requested if it is required. It will be necessary to agree and stipulate the duration, and whether it should extend beyond the warranty period, the cost and whether it includes the price of labour and spare parts, and the responsibilities of the owner and supplier.

There are a number of technical and environmental factors that need to be taken into account. For example:

  • If the area has an unstable power supply, is the supplier able to offer technical solutions (such as voltage stabilisers, an uninterruptible power supply)?
  • Will the geographical location (such as height above sea-level) affect the operation of equipment (such as motors, pressure vessels)? If so, can the manufacturer adjust the item’s specific needs?
  • Extremes of temperature, humidity, and dust may adversely affect equipment operation, and may require solutions such as air-conditioning, silica gel, polymerised coatings for printed circuit boards, and filters.

This information can be included within the generic equipment specifications. However, since much of the information is common to many pieces of equipment, some health service providers have found it simpler to develop a separate summary Technical and Environmental Data Sheet, which can be referred to in the purchase documents. This data sheet can be distributed to all suppliers, interested parties, trade delegations and other relevant bodies. Such a data sheet can be provided regardless of the length of specification or the procurement method used, ensuring that all parties are kept informed of prevailing national conditions which could affect the operation of equipment.

The following details should be included in a Technical and Environmental Data Sheet:

  • Electricity supply – mains or other supply, voltage and frequency values and fluctuations.
  • Water supply – mains or other supply, quality and pressure.
  • Environment: height above sea-level; mean temperature and fluctuations; humidity; dust level; vermin problems, etc.
  • Manufacturing quality – international or local standards required.
  • Language required – main and secondary.
  • Technology level required – manual, electro-mechanical or micro-processor controlled.

Evaluation and comparison process

The process of evaluation and comparison can often be time consuming. However, it is important to ensure that decisions for awarding contracts are not made simply on the basis of which items are the cheapest. During evaluation the items should be assessed against the requirements specified in the purchase document. The most common way to evaluate offers is to use an elimination process, where some offers are rejected at each stage. Offers should be judged against the following criteria:

  • Compliance with requirements in the purchase document.
  • Technical nature of the offer (part of the product selection criteria).
  • Financial nature of the offer (part of the product selection criteria).
  • Supplier qualification criteria.


By doing this, decisions are based on best value for money for the whole life-cycle cost, rather than simply being based on the item’s purchase price.

The process of evaluation and comparison must be fair and thorough. To achieve this, the process must follow a defined pattern to ensure all bids/quotes are dealt with in exactly the same way.

The evaluation process for tenders is similar to that for quotes, although the tender process is normally a far more comprehensive task and is also regulated by law. The tools for evaluation can be the same, but the amount of information required is usually much less with quotation methods. Obviously, if only three quotes are requested for a simple small order, the evaluation process should not take much time. The following evaluation steps are used, and some bids/quotes are rejected at the end of each step.


Step 1: Checking for compliance

The first step when evaluating offers is to determine which, if any, are not compliant with the technical, commercial, and other specifications in the purchase document. The procurement unit should be able to do this. It involves a more detailed examination of the offer to determine the compliance by the bidder with the requirements specified in the purchase document. This is known in tender processes as the substantial responsiveness of the bid. This process is more formal and comprehensive for tenders than for quotations.

A substantially responsive bid is one which:

  • conforms to all the terms and conditions; this means that the supplier has responded to all parts of the schedule of requirements, has filled in all the boxes, and is able to supply all the parts required; and
  • also establishes the bidder’s qualifications to supply and deliver the products within the delivery schedule; for example, the supplier:

- has enclosed signed audited accounts, signed company declarations on health, safety, and environmental activities, certificates of quality manufacturing, and a letter of authorisation from the manufacturer, and

- has nominated a representative in the country (if this was one of the compliance criteria).

All non-substantial bids will be rejected as non-responsive and should be excluded from further in-depth evaluation.

In practice it is found that most bids contain reservations from one or more of the detailed requirements. If these are just minor adjustments and do not represent a substantial deviation from expressed interests, one can still conclude that the bid is substantially responsive and therefore should be included. However, the reservations for closer clarification should be listed.

To assist in this examination one could ask for other clarifications from the bidder. One may also wish to inspect the quality methods and production methods stated in their documents. This request and response should be in writing. The bidders, however, are not allowed to make any changes to the substance or price of their offers. After evaluating the offers for compliance, some offers are discarded as the suppliers fail. The remaining offers can go forward to be compared in terms of technical performance (Step 3).

Step 2: Preparing the evaluation information

The procurement unit should collate and compile the information from all the responsive bids into evaluation information sheets. Box 10 gives an example of the sort of data that needs to be included.

Box 10: Evaluation information sheets

Evaluation Information Sheets present an easy way to compare different bids/quotes. For ease of comparison, it is best to allocate one page per subject matter (technical product details, price, etc.) and compare the offers side-by-side. Areas where each offer deviates from the equipment specification should be highlighted. Typical evaluation information sheets would include the following evaluation criteria:


Technical product data:

  • The international/regional standards that the equipment adheres to.
  • Whether the operational method used is new, well tried, or old.
  • The level of sophistication of the technology and the operating technique.
  • Which functions and measurements do not meet the specifications in the purchase document.
  • Whether any quality assurance certificates apply to the equipment.

Accessories, consumables, spare parts:

  • A list and the cost of accessories included in the offer.
  • A list and the cost of consumables included in the offer.
  • A list and the cost of spare parts included in the offer.
  • The length of time spare parts will be available and their location.

After-sales service:

  • Cost of after-sales support.
  • Guarantee/warranty periods.
  • The details of the after-sales support that can be provided.

Price information:

  • The price.
  • Delivery arrangements
  • Costs to install, commission, and train.
  • The life-cycle costs.

Note: this is an example and not a comprehensive list. The information chosen to include will depend upon the complexity of the equipment purchased – less technical detail is needed for simple equipment or recurrent supplies.


Ideally the evaluation information sheets should allow side-by-side comparison of the offers. For tenders there are more responses and the orders tend to be more complex, so more paperwork is required to obtain a true comparison. Usually there is too much information to be compiled in a single sheet, so it may be better to use:

  • one sheet for collating purely technical information about the product;
  • one for information on accessories, consumables, and spare parts;
  • one for after-sales service; and
  • one for price information.

The procurement unit should present the evaluation information sheets to the procurement/tender committee (for tenders and high-value quotes) or the Procurement Manager (for low-value quotes). They should be accompanied by an explanation of the requirements, main objectives, and any binding constraints. Then the technical evaluation process (Step 3) can commence.


Step 3: Carrying out the technical evaluation

The procurement/tender committee should base its decision on advice from members of the group with professional knowledge relevant to the offer. If appropriate, it should also seek advice from representatives from the relevant user department and HTM team (for low-value quotes, the Procurement Manager should also seek advice from these end-users).

The committee should consider the product selection criteria, as set out in the purchase document. It is essential that the information provided by the supplier is related only to the equipment specification and the selection criteria listed in the purchase document – any additional information intended to sway the evaluation can be seen as corruption; hence the importance of detailing requirements adequately in the purchase document. The better the purchase document, the easier the evaluation process will be. Box 11 lists a few points to remember, relating to the technical aspects of the offer.

Box 11: Summary technical assessment

  • If a detailed specification was issued, then every detail of the offer must be closely checked to make sure it conforms to the original specification.
  • If only a brief specification was issued, then the checks should be limited to ensuring the equipment or service offered meets the requirements.
  • Any modifications or alternatives offered must be assessed individually, and decisions made whether any one is more cost-effective than another.
  • The technical assessment includes suitability, safety, ability to commission and train, after-sales support, warranty arrangements and more – do not simply assess technical data concerning the equipment.

For both quotations and tenders it may be necessary to ask the supplier to clarify any ambiguities or uncertainties. Alternatively, a shortlist of suppliers can be drawn up and those included can be asked to demonstrate their equipment, as part of the technical evaluation (this is unlikely to be necessary for very simple equipment, and may be impossible for many overseas suppliers).

After the technical evaluation, some offers are discarded if they fail to meet the requirements. The remaining offers can go forward to be compared in terms of financial performance.