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
 

Problems with the Guidelines

Twelve out of 16 consolidators (75%) have experienced problems with the 12-month minimum shelf-life guideline, as compared with only 30% of donors and 27% of recipients (see Figure 3). Within the donor group 21% of the pharmaceutical industry had experienced problems with the provision. Comments mentioned the restrictive and arbitrary nature of the guideline, and rigidity in its use. Some recipient governments have given insufficient consideration to the possible exceptions, resulting in some valid donations being delayed or cancelled.


Figure 3. Percentage of respondents for whose organization the expiry date provision (Article 6) caused problems (n = 111)

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Last updated: May 3, 2013