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FDA Recent Draft Guidance Related to 21 CFR Part 11, Electronic Records/Signatures for Clinical Investigations
Overview: Companies engaged in human clinical trials must comply with specific regulatory requ..
Date : 01st February 2024
Time : This Event is Over and the Recorded Content is Available
Duration : 90 Mins
Clinical Trial Master File (TMF) and electronic Clinical Trial Master File (eTMF) and FDA Compliance
Overview: Companies engaged in the conduct of human clinical trials must adhere to specific g..
Date : 28th October 2022
Time : This Event is Over and the Recorded Content is Available
Duration : 90 Mins
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