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Trial Master File for Research Sites: Can You Pass FDA Inspection?

27 June 2012, Palo Alto, United States


Introduction
This webinar on Trial Master File (TMF) for clinical research sites will show how you can create an FDA compliant TMF to ensure that it will pass inspection by FDA investigators and QA Auditors.
Venue

2600 E. Bayshore Road, Palo Alto, 94303, United States

Organised by
ComplianceOnline
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