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July 10 , 2017

Health Canada recently released a discussion paper entitled Toward Mandatory Reporting of Serious Adverse Drug Reactions and Medical Device Incidents by Health Care Institutions.  The paper outlines a proposed approach to mandatory reporting by certain healthcare institutions of adverse drug reactions and medical device incidents.

Health Canada will be hosting a webinar on July 18th to share information and answer questions on the proposed regulations. To register for the webinar, please send your name and email address by Wednesday, July 12th to stakeholder webinar.

Health Canada is seeking written input on the proposed regulations. The 45-day consultation period runs until August 11, 2017. The consultations will inform the design of mandatory reporting regulations, and the education, outreach and feedback activities that will complement these regulations. Submit written input

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