First-Year Experiences with the Interagency Guidelines for Drug Donations
(2000; 51 pages)
Índice de contenido
Ver el documentoAcknowledgements
Ver el documentoExecutive summary
Abrir esta carpeta y ver su contenido1. Introduction
Cerrar esta carpeta2. Sources of information and study methodology
Ver el documentoGeneral overview of the method
Ver el documentoDefinition of respondents
Ver el documentoQuestionnaires
Ver el documentoDistribution of questionnaires
Ver el documentoInclusion criteria
Ver el documentoSample size
Ver el documentoData analysis
Abrir esta carpeta y ver su contenido3. Dissemination and uptake of the Guidelines
Abrir esta carpeta y ver su contenido4. Basic characteristics of drug donations
Abrir esta carpeta y ver su contenido5. Practical benefits as a result of the Guidelines
Ver el documento6. Drug donations which were hampered, delayed or cancelled
Abrir esta carpeta y ver su contenido7. Experiences and opinions regarding the 12-month shelf-life requirement
Abrir esta carpeta y ver su contenido8. Other suggestions to improve the Guidelines
Abrir esta carpeta y ver su contenido9. How could donation practice be further improved?
Ver el documento10. Summary of recommendations
Ver el documento11. Postscript
Ver el documentoReferences
 

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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Última actualización: le 3 mayo 2013