Trial Master File Requirements and Essential Regulatory Documents
October 12, 2018 - Online Event ON CA

Webinar Compliance

info@webinarcompliance.com
Phone: 416-915-4438\58

This course will cover various types of essential documentation, subject specific and non-subject specific, for clinical trials involving drugs, biologics and medical devices trials. The course will help define what should be maintained at a research site and Sponsors to promote adequate and accurate documentation in compliance with current regulatory requirements.

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