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Ms.Marie Dorat
Area Of Expertise : FDA
15 Years Of Experience
Marie Dorat, CQA, CAA is a QA/RA compliance, GxP Training and International product registration Consultant with 15 years experience in the Pharmaceutical/Medical Device & IVD Industry She also is the CEO of IPRF, LLC which specializes in helping established and start-up companies process the necessary documents for international product distribution. She is also Managing Partner at iComplyRegs, LLC which provides the most current FDA/EU/ROW regulatory requirements updates as well as experienced RA/QA Consultants
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Recorded Webinar
Clinical Monitoring – GCP Trial Expectations
This course will provide guidance on best practices for conducting monitoring visits. We will explore strategies for dealing with common clinical trial monitoring issues. The course also summarizes the essential documentation required during the clinical trial and g ...
- Basic & Intermediate
- 60 Mins