First-Year Experiences with the Interagency Guidelines for Drug Donations
(2000; 51 pages)
Table of Contents
View the documentAcknowledgements
View the documentExecutive summary
Open this folder and view contents1. Introduction
Open this folder and view contents2. Sources of information and study methodology
Open this folder and view contents3. Dissemination and uptake of the Guidelines
Open this folder and view contents4. Basic characteristics of drug donations
Open this folder and view contents5. Practical benefits as a result of the Guidelines
View the document6. Drug donations which were hampered, delayed or cancelled
Close this folder7. Experiences and opinions regarding the 12-month shelf-life requirement
View the documentImpact of the Guidelines
View the documentGuidelines by other organizations
View the documentAgreement with the current provision
View the documentProblems with the Guidelines
View the documentArguments for and against the 12-month shelf-life provision
View the documentRecommendations
Open this folder and view contents8. Other suggestions to improve the Guidelines
Open this folder and view contents9. How could donation practice be further improved?
View the document10. Summary of recommendations
View the document11. Postscript
View the documentReferences
 

Guidelines by other organizations

All governments and organizations that developed national or institutional guidelines on the basis of the Guidelines maintained the 12-month minimum shelf-life requirement, sometimes with exceptions (see Table 2).

Table 2. Minimum shelf-life upon arrival, as formulated in other guidelines

Italy, Netherlands, Norway, United Republic of Tanzania

12 months, same exceptions as Guidelines

Australia, Zimbabwe

12 months, no exceptions

International Pharmaceutical Federation

Should normally be 12 months; when a shorter shelf-life is appropriate, the donor is responsible for informing the recipient and for ensuring that the remaining shelf-life allows for proper administration

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Last updated: May 3, 2013