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
Close this folder2. Sources of information and study methodology
View the documentGeneral overview of the method
View the documentDefinition of respondents
View the documentQuestionnaires
View the documentDistribution of questionnaires
View the documentInclusion criteria
View the documentSample size
View the documentData analysis
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
Open this folder and view contents7. Experiences and opinions regarding the 12-month shelf-life requirement
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
 

Questionnaires

The questionnaires were prepared specifically for donors, consolidators and recipients. Definitions were placed at the beginning of each questionnaire to help organizations to identify themselves as a donor or a consolidator. The opinions of recipients were actively solicited, and donors and consolidators were encouraged to send copies of the questionnaire to their recipient partners, and to request their opinions.

The questions were divided into "closed questions" with a yes/no response and "open-ended questions" which allowed respondents freedom and space to formulate their replies and comments. The sequence followed as much as possible that of the Guidelines themselves and the overriding intention was to allow respondents sufficient space to express their opinions on any aspect of the Guidelines.

Copies of the draft questionnaires were first sent to 12 representative organizations, with a request for their comments and observations. Four were interagency co-sponsors of the Guidelines. The questionnaires were modified in the light of comments. French versions of the three questionnaires were also produced and distributed.

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Last updated: May 3, 2013