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Guidelines for drug donations
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Sponsors of these guidelines for drug donations are:
Caritas InternationalisChurches' Action for Health of the World Council of Churches
International Committee of the Red Cross
International Federation of Red Cross and Red Crescent Societies
International Pharmaceutical Federation
Joint United Nations Program on HIV/AID
Médecins Sans Frontières
Office of the United Nations High Commissioner for Refugees
OXFAMPharmaciens Sans FrontièresUnited Nations Children's FundUnited Nations Development ProgramUnited Nations Population FundWorld BankWorld Health Organization Introduction
I - The need for guidelines
II - Core Principles
III - Guidelines for drug donations
Selection of drugs Quality assurance and shelf-life
Presentation, packing and labeling Information and management
IV - Other ways donors can help
The New Emergency Health Kit Donations in cash
Additional guidelines for drug donations as part of development aid
V - How to implement a policy on drug donations
Management of drug donations by the recipient
Actions required from donor agencies
References
AcknowledgmentsIntroduction These Guidelines for drug donations have been developed by the World Health Organization (WHO) in cooperation
with the major international agencies active in humanitarian relief. The first version was issued in May 1996 and represented the consensus of WHO, Churches' Action for Health of the World Council of Churches, the
International Committee of the Red Cross, the International Federation of Red Cross and Red Crescent Societies, Médecins Sans Frontières, the Office of the United Nations High Commissioner for Refugees, OXFAM and the
United Nations Children's Fund. In 1999 the number of co-sponsors expanded to include Caritas Internationalis, the International Pharmaceutical Federation, Pharmaciens Sans Frontières, UNAIDS, the United Nations
Development Program, the United Nations Population Fund and the World Bank.The Guidelines aim to improve the quality of drug donations, not to hinder them. They are not an
international regulation, but are intended to serve as a basis for national or institutional guidelines, to be reviewed, adapted and implemented by governments and organizations dealing with drug donations.
The original Guidelines
were based on several rounds of consultation and comments by over 100 humanitarian organizations and individual experts. In 1996 WHO was requested by the World Health Assembly, in resolution WHA49.14, to review the
experiences with the guidelines after one year. In autumn 1997 WHO's Action Program on Essential Drugs therefore initiated a global review of first-year experiences. The results of the review are presented in the
forthcoming document First-year experiences with the interagency guidelines for drug donations. The evaluation formed the basis for the changes in the text. In general, experiences with the Guidelines were very
positive. But there were complaints that the authorities in some recipient countries strictly adhered to the Guidelines, without regard for the exceptions specifically included, and as a result useful donations were
lost. For example, problems were reported with Guideline 6: "donated drugs should have a remaining shelf-life of 12 months upon arrival in the recipient country". However, the problems arose from
misunderstanding of or failure to refer to the stated exceptions to that guideline, rather than from the text of Guideline 6 itself. In this revised edition Guideline 6 has been modified. It now allows for direct
donations of drugs with a remaining shelf-life of less than one year to specific health facilities, provided assurance can be given that the drugs can be used prior to expiration.There are many different scenarios for drug
donations. They may take place in acute emergencies or as part of development aid in non-emergency situations. They may be corporate donations (direct or through private voluntary organizations), aid by governments, or
donations aimed directly at single health facilities. And although there are legitimate differences between these scenarios, there are many basic rules for an appropriate donation that apply to all. The Guidelines aim
to describe this common core of "Good Donation Practice".This document starts with a discussion on the need for guidelines, followed by a presentation of the four
core principles for drug donations. The guidelines for drug donations are presented in Chapter IV. When necessary for specific situations, possible exceptions to the general guidelines are indicated. Chapter V gives
some suggestions on other ways that donors may help, and Chapter VI contains practical advice on how to implement a policy on drug donations.
I. The need for guidelines.
These Guidelines are not international regulations; they are intended to serve as a basis for national or institutional guidelines, to be reviewed, adapted and implemented by governments and
organizations dealing with drug donations. In the face of disaster and suffering there is a natural human impulse to reach out and help those in need.
Medicines are an essential element in alleviating suffering, and international humanitarian relief efforts can greatly benefit from donations of appropriate drugs.Unfortunately, there are also many examples of drug donations which cause
problems instead of being helpful. A sizable disaster does not always lead to an objective assessment of emergency medical needs based on epidemiological data and past experience. Very often an emotional appeal for
massive medical assistance is issued without guidance on what are the priority needs. Numerous examples of inappropriate drug donations have been reported (see Annex). The main problems can be summarized as follows:
Donated drugs are often not relevant for the emergency
situation, for the disease pattern or for the level of care that is available. They are often unknown by local health professionals and patients, and may not comply with locally agreed drug policies and standard
treatment guidelines; they may even be dangerous.
Many donated drugs arrive unsorted and labeled in a language which is not easily understood. Some donated drugs come under trade names which are not registered for use in the recipient country, and
without an International Nonproprietary Name (INN, or generic name) on the label.
The quality of the drugs does not always comply with standards in the donor country. For example, donated
drugs may have expired before they reach the patient, or they may be drugs or free samples returned to pharmacies by patients or health professionals.
The donor agency sometimes ignores local administrative procedures for receiving and distributing medical supplies. The distribution plan of the donor agencies may conflict with the wishes of national authorities.
Donated drugs may have a high
declared value, e.g. the market value in the donor country rather than the world market price. In such cases import taxes and overheads for storage and distribution may be unnecessarily high, and the (inflated) value of
the donation may be deducted from the government drug budget.
Drugs may be donated in the wrong quantities, and some stocks may have to be destroyed. This is wasteful and creates problems of disposal at the receiving end.
There are several underlying reasons for these
problems. Probably the most important factor is the common but mistaken belief that in an acute emergency any type of drug is better than none at all. Another important factor is a general lack of communication between
the donor and the recipient, leading to many unnecessary donations. This is unfortunate because in disaster situations and war zones inappropriate drug donations create an extra workload in sorting, storage and
distribution and can easily over stretch the capacity of precious human resources and scarce transport volume. Often, the total handling costs (duties, storage, transport) are higher than the value of the drugs.
Stockpiling of unused drugs can encourage pilfering and black market sales.Donating returned drugs (unused drugs returned to a pharmacy for safe disposal, or free samples given to
health professionals) is an example of double standards because in most countries their use would not be permitted due to quality control regulations. Apart from quality aspects, such donations also frustrate management
efforts to administer drug stocks in a rational way. Prescribers are confronted with many different drugs and brands in ever changing dosages; patients on long-term treatment suffer because the same drug may not be
available the next time. For these reasons this type of donation is forbidden in an increasing number of countries and is generally discouraged.In the early 1980s the first guidelines for drug donations were developed by international
humanitarian organizations, such as the International Committee of the Red Cross (ICRC) and the Christian Medical Commission (CMC) of the World Council of Churches, later called Churches' Action for Health. In 1990 the
WHO Action Program on Essential Drugs, in close collaboration with the major international emergency aid agencies, issued a first set of WHO guidelines for donors (1) later refined by the WHO Expert Committee on the Use of Essential Drugs.(2) In 1994 the WHO office in Zagreb issued specific guidelines for humanitarian assistance to former Yugoslavia.(3) In view of the existence of these different drug donation guidelines the need was felt for one comprehensive
set of guidelines that would be endorsed and used by all major international agencies active in emergency relief. For this reason a first draft was prepared by the WHO Action Program on Essential Drugs and further
refined in close collaboration with the division of Drug Management and Policies and the division of Emergency and Humanitarian Action, major international relief organizations and a large number of international
experts. The final text represents the consensus between the World Health Organization, UNICEF, the Office of the United Nations High Commissioner for Refugees, the International Committee of the Red Cross, the
International Federation of Red Cross and Red Crescent Societies, Churches' Action for Health of the World Council of Churches, Médecins sans Frontières and OXFAM. In the process comments by over 100 humanitarian
organizations and individual experts were taken into consideration.The examples of inappropriate donations quoted above constitute ample reasons to develop international
guidelines for drug donations. In summary, guidelines are needed because:
Donors intend well, but often do
not realize the possible inconveniences and unwanted consequences at the receiving end.
Donor and recipient do not communicate on equal terms. Recipients may need support in specifying how they want to be helped.
Drugs do not arrive in a
vacuum. Drug needs may vary between countries and from situation to situation. Drug donations must be based on a sound analysis of the needs, and their selection and distribution must fit within existing drug
policies and administrative systems. Unsolicited and unnecessary drug donations are wasteful and should not occur.
The quality requirements of drugs are different from other donated items, such as food and clothing.
Drugs can be harmful if misused, they need to be identified easily through labels and written information, they may expire, and they may have to be destroyed in a professional way.
II - Core Principles
The twelve articles of the
Guidelines for Drug Donations are based on four core principles. The first and paramount principle is that a drug donation should benefit the recipient to the maximum extent possible. This implies that all donations
should be based on an expressed need and that unsolicited drug donations are to be discouraged. The second principle is that a donation should be given with full respect for the wishes and authority of the recipient,
and be supportive of existing government health policies and administrative arrangements. The third principle is that there should be no double standards in quality: if the quality of an item is unacceptable in the
donor country, it is also unacceptable as a donation. The fourth principle is that there should be effective communication between the donor and the recipient: donations should be based on an expressed need and should
not be sent unannounced. Justification and explanation
This provision stresses the point that it is the prime responsibility of the recipients to specify their needs. It is intended to prevent unsolicited donations,
and donations which arrive unannounced and unwanted. It also empowers the recipients to refuse unwanted gifts.
Possible exceptions
In acute emergencies the need for prior consent by the recipient may be waived,
provided the drugs are amongst those from the WHO Model List of Essential Drugs(4) that are included in the UN list of emergency relief items recommended for use in acute emergencies.(5) Core principles of a donation
Maximum benefit to the recipient
Respect for wishes and authority of the recipient
No double standards in quality
Effective communication between donor and recipient
III - Guidelines for drug donations
Selection of drugs
1. All drug donations should be based on
an expressed need and be relevant to the disease pattern in the recipient country. Drugs should not be sent without prior consent by the recipient.2. All donated drugs or their generic equivalents should be approved for use in the recipient country
and appear on the national list of essential drugs, or, if a national list is not available, on the WHO Model List of Essential Drugs, unless specifically requested otherwise by the recipient.
Justification and explanation
This provision is
intended to ensure that drug donations comply with national drug policies and essential drugs programs. It aims at maximizing the positive impact of the donation, and prevents the donation of drugs which are unnecessary
and/or unknown in the recipient country.
Possible exceptions
An exception can be made for drugs needed in sudden outbreaks of uncommon or newly emerging diseases, since such drugs may not be approved for use in
the recipient country.
3. The presentation, strength and formulation
of donated drugs should, as much as possible, be similar to those commonly used in the recipient country.Justification and explanation
Most staff working at different health care levels in the recipient country
have been trained to use a certain formulation and dosage schedule and cannot constantly change their treatment practices. Moreover, they often have insufficient training in performing the necessary dosage calculations
required for such changes.
Quality assurance and shelf-life
4. All donated drugs should be obtained from a reliable source and
comply with quality standards in both donor and recipient country. The WHO Certification Scheme on the Quality of Pharmaceutical Products Moving in International Commerce(6) should be used.Justification and explanation
This provision prevents double standards: drugs of unacceptable quality in
the donor country should not be donated to other countries. Donated drugs should be authorized for sale in the country of origin, and manufactured in accordance with international standards of Good Manufacturing
Practice (GMP).
Possible exceptions
In acute emergencies the use of the WHO Certification Scheme may not be practical. However, if it is not used, a justification should be given by the donor. When donors provide
funds to purchase drugs from local producers, those which comply with national standards should not be excluded on the sole grounds that they do not meet quality standards of the donor country 5. No drugs should be donated that have been issued to patients and then returned to a pharmacy or
elsewhere, or were given to health professionals as free samples.Justification and explanation
Patients return unused drugs to a pharmacy to ensure their safe disposal; the same applies to drug samples that have been received by health
workers. In most countries it is not allowed to issue such drugs to other patients, because their quality cannot be guaranteed. For this reason returned drugs should not be donated either. In addition to quality issues,
returned drugs are very difficult to manage at the receiving end because of broken packages and small quantities involved. 6. After arrival in the recipient country all donated drugs should have a remaining shelf-life of at least
one year. An exception may be made for direct donations to specific health facilities, provided that: the responsible professional at the receiving end acknowledges that (s)he is aware of the shelf-life; and that the
quantity and remaining shelf-life allow for proper administration prior to expiration. In all cases it is important that the date of arrival and the expiry dates of the drugs be communicated to the recipient well in
advance.Justification and explanation
In many recipient countries, and especially under emergency situations, there are logistical problems. Very often the regular drug distribution system has limited possibilities for immediate distribution. Regular
distribution through different storage levels (e.g. central store, provincial store, district hospital) may take six to nine months. This provision especially prevents the donation of drugs just before their expiry, as
in most cases such drugs would only reach the patient after expiry. It is important that the recipient official responsible for acceptance of the donation is fully aware of the quantities of drugs being donated, as
overstocking may lead to wastage. The argument that short-dated products can be donated in the case of acute emergencies, because they will be used rapidly, is incorrect. In emergency situations the systems for
reception, storage and distribution of drugs are very often disrupted and overloaded, and many donated drugs tend to accumulate.
Additional exception
Besides the possible exception for direct donations mentioned
above, an exception should be made for drugs with a total shelf-life of less than two years, in which case at least one-third of the shelf-life should remain. Presentation, packing and labeling 7. All drugs should be labeled in a language that is easily understood by health professionals in the
recipient country; the label on each individual container should at least contain the International Nonproprietary Name (INN, or generic name), batch number, dosage form, strength, name of manufacturer, quantity in the
container, storage conditions and expiry date.Justification and explanation
All donated drugs, including those under brand name, should be labeled also with their INN or the official generic name. Most training programs are based on the use
of generic names. Receiving drugs under different and often unknown brand names and without the INN is confusing for health workers and can even be dangerous for patients. In case of injections, the route of
administration should be indicated.
8. As much as possible, donated drugs should be presented in larger quantity units and hospital packs.
Justification and explanation
Large
quantity packs are cheaper, less bulky to transport and conform better with public sector supply systems in most developing countries. This provision also prevents the donation of drugs in sample packages, which are
impractical to manage. In precarious situations, the donations of pediatric syrups and mixtures may be inappropriate because of logistical problems and their potential misuse.9. All drug donations should be packed in accordance with international shipping regulations, and be
accompanied by a detailed packing list which specifies the contents of each numbered carton by INN, dosage form, quantity, batch number, expiry date, volume, weight and any special storage conditions. The weight per
carton should not exceed 50 kilograms. Drugs should not be mixed with other supplies in the same carton.Justification and explanation
This provision is intended to facilitate the administration, storage and
distribution of donations in emergency situations, as the identification and management of unmarked boxes with mixed drugs is very time and labour intensive. This provision specifically discourages donations of small
quantities of mixed drugs. The maximum weight of 50 kg ensures that each carton can be handled without special equipment. Information and management 10. Recipients should be informed of all drug donations that are being considered, prepared or actually underway.
Justification and explanation
Many drug
donations arrive unannounced. Detailed advance information on all drug donations is essential to enable the recipient to plan for the receipt of the donation and to coordinate the donation with other sources of supply.
The information should at least include: the type and quantities of donated drugs including their International Nonproprietary Name (INN or generic name), strength, dosage form, manufacturer and expiry date; reference
to earlier correspondence (for example, the letter of consent by the recipient); the expected date of arrival and port of entry; and the identity and contact address of the donor. 11. In the recipient country the declared value of a drug donation should be based upon the wholesale
price of its generic equivalent in the recipient country, or, if such information is not available, on the wholesale world-market price for its generic equivalent.Justification and explanation
This provision is needed in the recipient country to prevent drug
donations being priced according to the retail price of the product in the donor country, which may lead to elevated overhead cost for import tax, port clearance, and handling in the recipient country. It may also
result in a corresponding decrease in the public sector drug budget in the recipient country.
Possible exception
In case of patented drugs (for which there is no generic equivalent) the wholesale price of the
nearest therapeutic equivalent could be taken as a reference. 12. Costs of
international and local transport, warehousing, port clearance and appropriate storage and handling should be paid by the donor agency, unless specifically agreed otherwise with the recipient in advance.
Justification and explanation
This provision
prevents the recipient from being forced to spend effort and money on the clearance and transport of unannounced consignments of unwanted items, and also enables the recipient to review the list of donated items at an
early stage.IV - Other ways donors can help The New Emergency Health KitIn the acute phase of an emergency, or in the case of displacements of refugee populations without any
medical care, it is better to send a standardized kit of drugs and medical supplies that is specifically designed for this purpose. For example, the New Emergency Health Kit,(7) which has been widely used since 1990, contains drugs, disposable supplies and basic equipment needed for general medical care for a population of 10,000 for three months. Its contents are based on a consensus among the same group of major international aid agencies that also issued the drug donation guidelines. It is permanently stocked by several major international suppliers (for example, UNICEF and IDA) and can be available within 48 hours. It is especially relevant in the absence of specific requests.
Donations in cashAfter the acute phase of the emergency is over, a donation in cash for
local or regional purchase of essential drugs is usually much more welcome than further drug donations in kind. Such a cash contribution is very supportive to the activities of the local government or coordinating
committee, it is supportive to the local and regional pharmaceutical industry and it may also be more cost-effective. In addition, prescribers and patients are usually more familiar with locally produced drugs.
Additional guidelines for drug donations as part of development aid
When drug donations are given between
governments as humanitarian support to long-lasting complex emergencies and as regular development (commodity) aid there is usually more time to consider specific demands from the side of the recipient. On the other
hand, there is also time to link more restrictions to the donation, e.g. to products from manufacturers in the donor country, and to drugs registered for use in the recipient country.It should be recognized that drugs do not arrive in an administrative
vacuum. drug donations should not create an abnormal situation which may obstruct or delay national capacity building in selection, procurement, storage, distribution and rational use of drugs. Special care should
therefore be taken that the donated drugs respond to an expressed need, comply with the national drug policy, and are in accordance with national treatment guidelines in the recipient country. Administratively, the
drugs should be treated as if they were procured. This means that they should be registered or authorized for use in the country through the same procedure that is used for government tenders. They should be entered
into the inventory, distributed through the existing distribution channels and be subject to the same quality assurance procedures. If cost-sharing procedures are operational in the recipient country, the donated drugs
should not automatically be distributed free of charge. V - How to implement a policy on drug donations
Management of drug donations by the recipient
Define national guidelines for drug donations
It is difficult for a recipient to refuse a donation that has already arrived. Prevention is therefore better than cure. Recipients should indicate to their prospective donors what kind of assistance they need, and
how they would like to receive it. If this information is provided in a professional way, most donors will appreciate it and will comply. Therefore, recipients should first formulate their own national guidelines for drug donations, on the basis
of these international guidelines. They can also be included in the national drug policy. These national guidelines should then be officially presented and explained to the donor community. Only after they have been
presented and officially published can they be enforced.Define administrative procedures for receiving drug donations It is not enough for the recipient to adopt and publish the general guidelines on the selection, quality, presentation and management of
drug donations. Administrative procedures need to be developed by the recipient to maximize the potential benefit of drug donations. As much as possible such arrangements should be linked with existing drug supply
systems, but there are several questions which apply to donations only. Examples of such important questions, which have to be addressed in each country, are: Who is responsible for defining the needs, and who will prioritize them?
Who coordinates all drug donations?
Which documents are needed when a donation is planned; who should receive them?
Which procedure is used when donations do not follow the guidelines?
What are the criteria for accepting/rejecting a donation; who makes the final decision?
Who coordinates reception, storage and distribution of the donated drugs?
How are donations valued and entered into the budget/expenditure records?
How will inappropriate donations be disposed of?
Specify the needs for donated drugs The third
important action by the recipient is to specify the needs for donated drugs as much as possible. This puts the onus on the recipient to carefully prepare such requests, indicating the required quantities and
prioritizing the items. The more information given, the better. Information on donations that are already in the pipeline, or anticipated, is very helpful to other potential donors. Full information from the side of the
recipient is greatly appreciated by donors and pays off in the long run.Manage drugs with less than one-year expiry Drugs do not become toxic or ineffective on their date of expiry
but may slowly deteriorate depending on the product, formulation and storage conditions. Some become toxic but most simply lose their efficacy. An expiry date is the date given on the individual container (usually on
the label) of a drug product, up to and including which the product is expected to remain within specifications, if stored correctly. It is established for each batch by adding the shelf-life period to the date of
manufacture. The recommendation that all drugs should have a remaining shelf-life of at least one year upon arrival in a recipient country is to allow for the all too frequent in-country distribution delays. It gives a
measure of security that patients will receive drugs of good quality.A specific exception to the one-year shelf-life requirement can be made for donated drugs provided that: they
are direct donations to specific health facilities; the responsible professional acknowledges that (s)he is aware they are short-dated; and the quantity and the remaining shelf-life allow for proper administration,
distribution and prescription prior to expiry. Experience has shown that some recipient governments have applied the Guidelines very strictly, without due consideration of the possible exceptions to the general rule.
This has resulted in unnecessary impounding and disposal of valuable donations.Ensure rapid customs clearance of donated drugs Rapid customs clearance is required for all donated drugs.
Customs and health ministry officials managing drug donations covered by the Guidelines have the responsible task of allowing entry for useful donations, while rejecting short-dated donations for which satisfactory
distribution provisions have not been made.Manage donated drugs carefully The value of donated drugs can be considerable, and the gift should be treated with due care. On arrival the drugs should be inspected and their
receipt confirmed to the donor agency. They should then be stored and distributed in accordance with normal principles of good pharmacy practice and under the responsibility of adequately trained professionals. There
must be due vigilance to ensure that donated products are not diverted for export, commercial sale, or into illicit channels. Actions required from donor agencies Donors should always respect the four core principles for drug donations presented above. Donors
should also respect the national guidelines for drug donations and respond to the priority needs indicated by the recipient. Unsolicited donations should be prevented as much as possible. The public at large in the donor country is not always aware of the common
problems with drug donations. It is therefore important that governments in donor countries spend some effort to create more public awareness on "good donor practice". The best moment for this is probably at
the time of the public appeal through the media.Within the recipient country it is recommended that the different donors choose a "lead-donor" amongst themselves, who coordinates donor activities and who may also act as the central
contact point in discussions with the recipient government.The recipient country should supply as much information as possible on requested and approved donations. On the other hand, the donors themselves should also inform the recipient well in advance and
in great detail about which donations are coming, and when. This will greatly assist the coordinating body in the recipient country to plan for the proper reception of the donations, and to identify the need for
additional supplies.Avoid donations of drugs with short expiry dates
The fundamental problem of donated drugs with
short expiry dates has troubled recipients for many years. On the other hand, global experiences indicate that well-managed donor organizations and pharmaceutical companies are generally able to avoid donating products
with short expiry dates. Some large companies have product outreach programs under which products are specifically donated from normal inventories, on the basis of an agreed-upon schedule, to meet recipients' needs.
One objective of the Guidelines is to reduce
donations of drugs with short expiry dates through better inventory control on the part of donor companies and intermediaries, and through better communications. Donors and intermediaries should avoid donations of drugs
with short expiry dates as much as possible.Inform the public
The general public in the donor country is not
always aware of the common problems with drug donations. It is therefore important that governments in donor countries make some effort to create more public awareness on "good donor practice". The best moment
for this is probably at the time of the public appeal through the media. Establish donor coordination It is recommended that within the recipient country the different donors collaborate in the establishment of a coordinating body. In emergency situations this is
essential. This body should determine the needs, priorities, storage, logistics and distribution, and act as the central contact point in discussion with the recipient government authorities. The responsible government department should supply relief agencies
with as much information as possible about requested and approved donations. Conversely, relief agencies should keep the donor coordinating body and the responsible government department fully informed of the specific
identity, arrival dates, quantities, and expiry dates of donations. This will greatly assist the coordinating body in the recipient country to plan for the proper reception of the donations, and to identify the need for
additional supplies. Within donor
countries all organizations should likewise establish a coordinating body at headquarters level, to ensure that appropriate donation policies and processes are followed. The argument that products with short expiry dates can be donated in the
case of acute emergencies, because they will be used rapidly, is incorrect. In emergency situations the systems for reception, storage and distribution of drugs are very often disrupted and overloaded, and many donated
drugs tend to accumulate.
References
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Emergency Relief Items. Compendium of basic specifications, Volume 2: Medical supplies,
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The New Emergency Health Kit 98. Geneva: World Health Organization, 1998. WHO/DAP/90.1
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The New Emergency Health Kit. Geneva: World Health Organization, 1990. WHO/DAP/98.10
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The use of essential drugs. Geneva: World Health Organization, 1992. Technical Report
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Medical supplies donor guidelines for WHO humanitarian assistance for former Yugoslavia.
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Acknowledgments The following persons and organizations are thanked for their comments and other contributions to the evaluation and
revision of the Guidelines: their help is gratefully acknowledged.N.D.Achu (Commonwealth Pharmaceutical Association, Cameroon), M.G.Andersen (Rotary Australia), S.Anderson (Astra
Pharmaceuticals Pty. Ltd., Australia), Sr. Angelina (Trinity Hospital, Malawi), B.Assam (South West Provincial Special
Fund for Health, Cameroon), S.Barbereau (Pharmaciens Sans Frontières, Comité International, France), B.Barnes
(Glaxo Wellcome plc., UK), P.G.Bindokas (Humanitarian Aid Commission, Lithuania), L.Blok (MSF, Holland), O.Brasseur
(International Centre for Childhood and the Family, France), A.Brúzas (Order of Malta, Lithuania), F.Bürger & K
.Zwingenberger (Grünenthal GmbH, Germany), K.Carter & J.Desautelle (AmeriCares, USA), J.Chamousset (Order of
Malta, Benin), L.S. Charimari (Provincial Medical Directorate, Zimbabwe), N.Chebotarenco (Association "Drugs", Republic
of Moldova), P.M.Chenaparampil (Alleppey Diocesan Charitable and Social Welfare Society, India), A.Chidarikire
(Ministry of Health and Child Welfare, Zimbabwe), J.C.Chin Loy (Sisters of the Poor, Philippines), Z.Chlap (Order of
Malta, Poland), B.D.Colatrella (Merck & Co. Inc., USA), D.Collier (Janssen Pharmaceutica, Belgium), E.M.Connolly
(Hoechst Marion Roussel Inc., USA), G.Coughlin (Order of Malta, El Salvador), A.Damdinsuren (Agency for Quality
Assurance of Drugs, Mongolia), R.A.Davey (Memorial Christian Hospital, Bangladesh), C.Dedza (Mlambe Hospital,
Malawi), C.Dick (Ekwendeni Hospital, Malawi), L.Dindonis (International Veterinary Educational Assistance, USA), K.Ditz
(Merck KGaA, Germany), D.Djamilatou (PEV/SSP/ME, Conakry, Guinea), C.Drown, (Medical Supplies Department, Nepal),
T.Dubuque (Crudem Foundation, USA), R.B.Elens (Holy Family Hospital, Malawi), K.Ellerbroek (Bayer AG, Germany), A.J
.Elphick (Novo Nordisk A/S, Denmark), A.Fadoul (Centers for Development and Health, Haiti), G. Fiorentino (Order of
Malta, Panama), G.Folkedal (Norway), G.-B.Forte (WHO/EURO), M.Gastellu Etchegorry (MSF, France), Cpt. N.Gaza (MOD,
Zimbabwe), G.Gedevanishvili (UMCOR, Georgia), R.Geursen & G.Küsters (Hoechst Marion Roussel, Germany), P.A.
Gibson (Eli Lilly and Company, USA), J.Glenn (SmithKline Beecham, USA), M.Greiff (Intercare, UK), F.C.Griz-Tesorero
(Order of Malta, Chile), C.Gursky (Bayer Corporation, USA), S.Gvörgy (Malteska Dobrotvorna Organizacija, Jugoslavije),
H.Haga (Nippon Glaxo Ltd.), M.Healy (Trócaire, Ireland), E.Hesse (MSF, Luxembourg), H.Hoppe (Bristol-Myers Squibb
GmbH, Germany), Horizons Santé (Cameroon), B.Irvine (Pharmaceutical Society of New Zealand), B.Jøldal (Sandvika
Apotek, Norway), P.A.Jotterand (Pharmaciens Sans Frontières, Comité International, France), K.Kafidi (Ministry of
Health and Social Services, Namibia), T.Kaneko (Kirin Brewery Co. Ltd., Japan), J.P.Kelsall (MAP International, Canada),
R.V.Kesteren-Archen (International Pharmaceutical Federation, Netherlands), H.Kienzl (Zeneca GmbH, Germany), G
.Kimball (UMCOR, Haiti), W.Kollmann (Knoll AG, Germany), W.Kotkowski (Sihanouk Hospital Centre of HOPE, Cambodia
), J.Krauskopf (Order of Malta, Croatia), C.E.Kuhinka (Wyeth-Ayerst Pharmaceuticals, USA), M.Kurian (Christian Medical
Commission, Churches' Action for Health, World Council of Churches, Switzerland), E.Larsson (DANIDA, Kenya), J.F
.Ledesma (St. Luke's Medical Centre, Philippines), P.Le Jacq (Maryknoll Missioners, United Republic of Tanzania), D
.Lejoyeux (Tulipe, France), J.P.Lepers (Institut Léprologie Appliquée, Senegal), D.Lockyer (Overseas Pharmaceutical Aid
for Life, Australia), J.-D.Lormand (MSF, Switzerland), A.Lungu (Swaziland), J.McDonald (St. Vincent de Paul Society,
Australia), H.Maisano (World Vision, Australia), J.Mamedov (UMCOR, Azerbaijan), A.Masel & K.-J. Schlabe (Berlin
-Chemie AG, Germany), F.Matthys (MSF, France), S.Meier (MAP International, USA), M.Minkaila (Direction Nationale de
la Santé Publique, Mali), A.Møller (Leo Pharmaceutical Products Ltd. A/S, Denmark), Mongolemimpex (Mongolia), C
.Mugadza (Datlabs Pvt. Ltd., Zimbabwe), C.Y.Mwasha (Muhimbili Health Centre, United Republic of Tanzania), Y.Nakano
(Fujisawa Pharmaceutical Co., Ltd., Japan), G.Nanu (Cible, Cameroon),), H.Norikyo & I.Kitamaru (Fuso Pharmaceutical
Industries Ltd., Japan), M.O'Donohue (Catholic Medical Mission Board Inc., USA), G.B.Okelo (University of Tropical
Medicine and Technology, Kenya), B.Olsen (International Federation of Red Cross and Red Crescent Societies,
Switzerland), E.M.A.Ombaka (Pharmaceutical Programme, Community Initiatives Support Services International, Kenya),
J.O'Neill (Save the Children Fund, Australia), Order of Malta, Dominican Republic, A.L.Oviedo (Ministerio de Salud y
Previsión Social de Bolivia), D.M.Padgett (Interchurch Medical Assistance Inc., USA), R.Paltridge (Crusade Mercy
Ministries, Australia), T.Parts (State Agency of Medicines, Estonia), B.Pastors (Action Medeor, Germany), C.Person
(Johnson and Johnson, USA), A.Petersen (DIFÄM, Germany), Pharmaceutical Product Donation Steering Committee
USA, The Pharmacist (Health Services Department, Zimbabwe), G.H. de Pommery (Oeuvres Hospitalières Françaises
de l'Ordre de Malte, France), W.L.Prelesnik (International Aid Inc., USA), S.K Proctor (Mayaka Health Centre, Malawi), F
.T.Puls (Memisa Medicus Mundi, Netherlands), N.Que (Christian Health Association of Malawi), M. Raijmakers (Wemos,
Netherlands), Ramakrishna Mission Ashrama (India) Dr. Rakotomanana (Direction des Pharmacies, Madagascar), R.W
.Rice (Asian Outreach Australia Inc., Australia), E.J.Ridder (Ministry of Development Cooperation, Netherlands), J.Rigal
(MSF), C.C.Robert (Presbyterian Medical Institutions, Cameroon), M.C.Robert (Hôpital Général de Kinshasa, Democratic
Republic of the Congo), L.Rolver (Nycomed Amersham, USA), J.Roos (Centro de Obras Sociales, Peru), C.J.Rumball
(CAN MAP, Canada), J.Russo (Partnership for Quality Medical Donations, USA), Sr. Sabina (Our Lady of Providence
Hospital, India), Sadebay (Cameroon), H.Sandbladh (International Federation of Red Cross and Red Crescent Societies
, Switzerland), M.Sarkar (Community Development Medicinal Unit, India), H.Sassounian (United Armenian Fund, USA),
C.Saunders (UNFPA, USA), P.Saunders (Essential Drug Project, OXFAM, UK), R.Scharf (Institute of Haematology and
Blood Transfusion, Poland), J.Schmick (World Vision, USA), Cpt.Sekouba-Bangoura (Order of Malta, Guinea), N.S
.Snarskis (Order of Malta, Latvia), B.Snell (Macfarlane Burnet Centre for Medical Research, Australia), J.A.Soltz
(Prosalud, Bolivia), S. Sopczynski, (Medical Mission Sisters, Ethiopia), G.Stark (Kalene Mission Hospital, Zambia), U
.Suna (Evangelical Mission Hospital, India), J.Svendsen (Interagency Procurement Services Office, United Nations Development Programme, Denmark), G. Szalay (WHO/SUP/DBP), D.W.Tarkieh (Needy Children Centre of Africa
International, Ghana), L.Taylor (Kyrgyzstan), S.Teper (Ministry of Health and Social Welfare, Poland), D.Thierry (Centre
de Santé de Lagdo, Cameroon), K.Timmermans (WHO Office, Indonesia), M.Torongu (Commonwealth Pharmaceutical
Association, Zimbabwe), A.Toumi (Direction de la Pharmacie et du Médicament, Tunisia), United Nations Children's Fund
, Supply Division, Denmark, I.V.Valdés (Order of Malta, Chile), W.Vandersmissen (SmithKline Beecham, Belgium), N
.van der Veer (Akzonobel, Netherlands), L.Vanoyan (UMCOR, Armenia), M.VÃ zquez (MSF, Spain). R.S.Villonco (Order of
Malta, Philippines), J.Volkman & F.B.Bauer (Fondación San Gabriel, Bolivia), K. Weerasuriya (Department of
Pharmacology, University of Colombo, Sri Lanka), D.Whyms (DFID, Bolivia), R.Wood (Samaritans Purse - World Medical Mission, USA), G.Zeana & F.Ionescu (Asociatia Salvavita, Romania). Copyright (c) World Health Organization 1999This document is issued by the WHO Department of Essential Drugs and Other Medicines. Comments and suggestions
for future revisions are welcome and can be sent to: The Director, Department of Essential Drugs and Other Medicines, World Health Organization, 1211 Geneva 27, Switzerland.The original document is not a formal publication of the World Health Organization (WHO), and all rights are reserved
by the Organization. The document may, however, be freely reviewed, abstracted, reproduced and translated, in part or
in whole, but not for sale nor for use in conjunction with commercial purposes. The views expressed in documents by named authors are solely the responsibility of those authors. |
