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DIA Canadian Pharmacovigilance & Risk Management Meeting

This 1-day meeting will provide new insights into the current issues and associated challenges impacting drug safety in Canada. Expert pharmaceutical, biotechnology, and regulatory thought leaders will discuss Regulatory Guidance Document Updates, the impact of Bill C-17 on adverse drug reaction reporting, Pharmacovigilance (PV) Agreements, eReporting, Special Product Areas; and much more. f

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