Adverse Reaction Information - How To Report

	Draft Guidance Document for Industry - Reporting Adverse Reactions to Marketed Health Products Date: 2006-10-30
	Canadian Adverse Drug Reaction Monitoring Program (CADRMP) Guidelines for the Voluntary Reporting of Suspected Adverse Reactions to Health Products by Health Professionals and Consumers Date: 2006-05-11

	Draft Guidance Document: Submission of Pharmacogenomic Information Date: 2006-03-07
	Guidance Document for Industry:Issuance of Health Professional Communications and Public Communications by Market Authorization Holders
	Guidelines for the Canadian Pharmaceutical Industry on Reporting Adverse Reactions to Marketed Drugs (Vaccines Excluded) Date: 2001-07-01
	Vaccines: Guidelines for Reporting Adverse Events Associated with Vaccine Products
	Reporting of Adverse Drug Reactions - clarifications
	Medical Devices Inspectorate
	Medical Devices: Mandatory and Voluntary Problem Reporting for Medical Devices
	Medical Devices: Product Recall Procedures


	Last Updated: 2006-11-22		Important Notices