Good clinical practices: Guidance documents
- Guidance Document: Part C, Division 5 of the Food and Drug Regulations "Drugs for Clinical Trials Involving Human Subjects" (GUI-0100)
- Risk classification guide for observations related to inspections of clinical trials of human drugs (GUI-0043)
- Annex 13 to the Good manufacturing practices guide for drugs used in clinical trials (GUI-0036)
- POL-0030: Compliance and enforcement approach and inspection strategy for clinical trials of drugs involving human subjects
- International Conference on Harmonization GCP - ICH E6