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Health Canada
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2017-05-04
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Drugs and health products legislation and guidelines
ARCHIVED - Legislation and Guidelines - Biologics, Radiopharmaceuticals and Genetic Therapies - Health Canada
Compliance and Enforcement - Legislation and Regulatory Amendments - Drugs and Health Products - Health Canada
Medical Devices
Natural Health Products
ARCHIVED - Development of a Regulatory Framework for Mandatory Reporting by Healthcare Institutions (Vanessa's Law)
ARCHIVED: Amendments to the Food and Drugs Act: Guide to New Authorities (power to require and disclose information, power to order a label change and power to order a recall )
Protecting Canadians from Unsafe Drugs Act (Vanessa's Law) Amendments to the Food and Drugs Act (Bill C-17)
Protecting Canadians from Unsafe Drugs Act (Vanessa's Law): Questions/Answers
ARCHIVED - Consultation on the Amendments to the Food and Drugs Act: Guide to New Authorities - What We Heard
Implementation of Vanessa-s Law
ARCHIVED - 2016 Protecting Canadians from Unsafe Drugs Act Transparency Needs-based Assessment: What We Heard
Overview of Vanessa's Law
Transparency Measures
Veterinary Drugs
Drug Products
Guide to authorities under the Protecting Canadians from Unsafe Drugs Act (Vanessa’s Law): Overview
Environmental risk management amendments to the Food and Drugs Act
Precision regulating: Amendments to the Food and Drugs Act
