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Essential Regulatory Documents and Regulatory Requirements for Biomedical Products

7th December 2018   -   7th December 2018
Fremont - online, United States
https://www.traininng.com/webinar/essential-regulatory-documents-and-regulatory-requirements-for-biomedical-products-200444live?conference-service-seo
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Abstract

Essential documentation serves to demonstrate the compliance of the investigators, Sponsors, monitors/CROs, and IRBs with the current regulatory requirements and ICH GCP standards. Techniques on how to develop best practices and meet all applicable regulatory requirements will be discussed.

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