Normative Documents

Normative Documents

Health Canada Food and Drugs Act
Personal Information Protection and Electronic Documents Act (PIPEDA)
Health Canada Food and Drugs Regulations, Part C, Division 5
Health Canada Natural Health Products Regulations, Part 4
Health Canada Medical Device Regulations, Part 3
Tri-Council Policy Statement: Ethical Conduct for Research Involving Humans – TCPS 2 (2018)
International Council for Harmonization (ICH) of Technical Requirements for Pharmaceuticals for Human Use Good Clinical Practice Guideline
US Code of Federal Regulations Title 21
US Code of Federal Regulations Title 45
A Systems Approach to Human Research Protection: Innovation in Healthcare, authored by Alexander G. Karabanow, BSc, BAA; Janice E. Parente, BSc, PhD; Jacquelyn Legere, RN, BN,CIPP/C; Ann Munro Heesters, BEd, BA(Hons.), MA, PhD
Institute of Medicine – Preserving Public Trust: Accreditation and Human Research Participant Protection Programs
Report on the Evaluation of Control Mechanisms in Clinical Research in Quebec (The Deschamps Report), authored by Pierre Deschamps, BCL, CM
The Governance of Health Research Involving Human Subjects (HRIHS), authored by Michael McDonald, BA, MA, PhD
World Health Organization – Standards and Operational Guidance for Ethics Review of Health-Related Research with Human Participants
World Medical Association – Declaration of Helsinki – Ethical Principles for Medical Research Involving Human Subjects