Health Canada
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Drugs and Health Products
What's New - 2013
- List of Canadian Establishments that Process and/or Import Semen for Assisted Conception [2013-06-17]
- Quality System Framework - Summary [2013-05-17]
- Guidance on Drug Establishment Licences and Drug Establishment Licensing Fees (GUI-0002) [2013-04-01]
- Guidance on Medical Device Establishment Licensing and Medical Device Establishment Licence Fees (GUI-0016) [2013-04-01]
- Guidance Document on the application for a Certificate of Pharmaceutical Product (GUI-0024) [2013-04-01]
- Frequently Asked Questions (FAQ's) - Drug Establishment Licensing and Fees [2013-04-01]
- Frequently Asked Questions (FAQs) - Medical Device Establishment Licensing and Fees [2013-04-01]
- Drug Establishment Licence Application Completion Checklist [2013-03-15]
- Drug Establishment Licence - Calculation Chart [2013-03-15]
- Part C: Canadian Warehouse Form [2013-03-15]
- Good Manufacturing Practices - Foreign Site Submission Form - Section 5 (FRM-0212) [2013-03-15]
- Consultation: Invitation to Participate in the Survey for ICH Q7 Constituencies Input for Development of a Question and Answer Document [2013-02-15]
- Good Pharmacovigliance Practices (GVP) [2013-02-11]
- Notice to Stakeholders: Name change for the Post-Market Reporting Compliance (PMRC) inspection program to Good Pharmacovigilance Practices (GVP)
- Good Pharmacovigilance Practices (GVP) Guidelines (GUI-0102)
- Risk Classification of Good Pharmacovigilance Practices (GVP) Observations (GUI-0063)
- Inspection Strategy for Good Pharmacovigilance Practices for Drugs (POL-0041)
- Drug and Medical Device Recall Listings [2013-02-04]
- The Inspectorate's Natural Health Products Compliance and Enforcement Policy (POL-0044) [2013-01-31]
- Summary Report of Inspections of Cells, Tissues and Organs Establishments Conducted from August 2009 to June 2012 [2013-01-16]
- Guidance on the Medical Device Inspection Programme (GUI-0064) [2013-01-11]
- Policy for the Inspection of Medical Device Companies (POL-0035) [2013-01-11]
- Summary Report: Stakeholder Consultation Workbook for the Medical Devices Inspection Cycle [2013-01-11]
