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International
Topics
Export & Import
Mutual Recognition Agreements
Partnerships
Regulatory Agencies
International
MRA - Mutual Recognition Agreements on Drugs/Medicinal Products Good Manufacturing Practices Compliance Programmes
Background
MRAs Updates
Internationally Harmonized Requirements for Batch Certification
Standard Operational Procedure for the Determination of Equivalency of Inspection Methods
Partnerships
PIC/S - Pharmaceutical Inspection Co-operation Scheme
Guidance on Parametric Release - Pharmaceutical Inspection Co-operation Scheme (PIC/S)
Http://www.picscheme.org
WHO - World Health Organization
http://www.who.int/home-page/
ICH - International Conference on Harmonization
http://www.ich.org
GHTF - Global Harmonization Task Force
http://www.ghtf.org/
OMCL - Official Medicines Control Laboratories
Regulatory Agencies
FDA - Food and Drug Administration - United States of America
TGA - Therapeutic Goods Administration - Australia
AGENCE Francaise de Securite Sanitaire des Produits de Sante - France
Medical Product Agency - Sweden
Medicines Control Agency - United Kingdom
European Commission - Enterprise DG Pharmaceuticals - Regulatory frameworks / Market authorisations
European Agency for the Evaluation of Medicinal Products
Export and Import
Guidance Document on the Application for Certificate of a Pharmaceutical Product (GUIDE-0024)
Policy on Importations of Drugs for Human Use including Natural Health Products into Canada (POL-0019)
Intention to Invoke Section 37 of the Canada Food and Drugs Act for Products being Exported
Site Reference File Guideline
Request for Stamping
Taking Medicine Across Borders
Policy for the Importation or Sale of Active Pharmaceutical Ingredients for Veterinary Use
Last Updated: 2006-04-12
Important Notices