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Clinical Trials in Canada: A Regulatory Review


Apr 24, 2010 8:00am ‐ Apr 24, 2010 9:00am



Credits: None available.

Description

This is an overview of current clinical trial regulations and guidance documents in Canada, including Division 5 of the Food and Drugs Regulations, ICH GCP E6, and related guidances, such as the importation policy, labelling of investigational products, and the unique Health Canada requirements for clinical trial record retention.

Speaker(s):

  • Patricia Jones, ART, RAC, Director, Quality and Regulatory Compliance, Therapeutic Products, Inc. (TPIreg)

Speaker(s):

Credits

Credits: None available.

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