September 21, 2017 8a PT/ 11a ET

Good Documentation Practice (GDP) is the cornerstone to ensuring a quality, inspection ready Trial Master File (TMF). GDP is the responsibility of everyone that contributes (i.e. via submission or creation) clinical trial documentation to the TMF.

This webinar evaluated the following:

  • The regulations that support GDP
  • Best practices on how document contributors can apply the golden rule of research to their TMF
  • How to avoid writing too many and unnecessary Note-to-Files (NTFs)
  • Tips on becoming inspection ready and staying that way

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