Revision of Technical Report No. 52: Guidance for Good Distribution Practices for the Pharmaceutical Supply Chain

This opportunity is for the revision of TR 52: Guidance for Good Distribution Practices for the Pharmaceutical Supply Chain. PDA technical documents rely on the contributions of industry subject matter experts and undergo external review to provide high-quality, valuable resources for the pharmaceutical industry. Authors from all experience levels and geographies are encouraged to participate to ensure the documents are accessible and relevant to a broad audience.

This is a virtual postion.

Please note this opportunity is available to members only.

If you are interested in joining this task force, please submit your application by completing the survey.