Mandatory Reporting of Serious Adverse Drug Reactions and Medical Device Incidents by Health Care Institutions

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Mandatory Reporting of Serious Adverse Drug Reactions and Medical Device Incidents by Health Care Institutions
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Health Canada is seeking responses from all stakeholders on the proposals identified in this consultation paper. Submissions will help inform the design of the regulations as well as Health Canada's proposed approaches on outreach and education and providing meaningful feedback to health care institutions and health care professionals. The consultation is open for a 45 day comment period starting June 28, 2017 until August 11, 2017. All stakeholders are invited to submit their views by email, mail, or by completing our online questionnaire.

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