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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