Canada

Assisted Human Reproduction Act

Canada Gazette Part II

Classification Rules for Medical Devices

Clinical Trial Application

Food and Drugs Act

Food and Drugs Act Marijuana Exemption (Food and Drugs Act)Regulations

Food and Drug Regulations

Food and Drug Regulations Amendment – Part C Drugs (passage: 17 June 2001)

Health Canada Addendum to the ICH Guidance E11: Clinical Investigation of Medicinal Products in the Pediatric Population

Health Canada Adverse Reaction Information

Health Canada Consolidation of the Food and Drugs Act and Food and Drug Regulations

Health Canada Medical Devices Problem Reporting

Health Canada Natural Health Products Regulations Amendment Concerning Special Access Programme (SAP)

Health Canada Preparation of an Application for Investigational Testing - Medical Devices

Health Canada Regulatory Requirements Governing Drugs for Use in Clinical Trials in Canada [.pdf]

Medical Devices Regulations

Medical Devices Regulations – Letter to Stakeholders Regarding Proposed Amendments [.pdf]

Memorandum of Understanding - Tri-Councils

Natural Health Products Regulations

Regulatory Requirements Governing Investigations with Schedule C Drugs (Radiopharmaceuticals, Kits and Generators)

Personal Health Information Protection Act (Ontario)

Personal Information Protection and Electronic Documents Act (PIPEDA)

PIPEDA Organizations in the Province of Quebec Exemption Order

Tri-Council Policy Statement: Ethical Conduct for Research Involving Humans, 1998 (with 2000, 2002 updates)