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Introduction

This seminar will cover the organization of Health Canada as it relates to clinical trials and drug development, Canadian regulations governing the conduct of clinical trials in this country, the process for getting approval of clinical trials, requirements after approval of the trial, submission of safety data, inspections by Health Canada related to clinical trials, Good Manufacturing Procedures (GMP) requirements for clinical trials, the conduct of Phase IV clinical trials, and pending changes to the conduct of clinical trials in Canada. We will review requirements for drugs, biologics, gene therapy and natural health products.

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Venue

Courtyard Toronto Downtown

Courtyard Toronto Downtown, 475 Yonge Street Toronto Ontario M4Y 1X7 Canada, Toronto, M4Y 1X7, Canada

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Organised by

GlobalCompliancePanel

Contact information

Mr John Robinson
161 Mission Falls Lane, Suite 216, Fremont, CA 94539, USA, United States, Fremont, 94539, United States of America
1800 447 9407
Contact us by email

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