PIC/S (Pharmaceuticals Inspection Co-operation Scheme)
PIC/S Checklist
- Document History
- Introduction
- Scope
- Content of Site Master File
- General Information on the Manufacturer
- Contact Information on the Manufacturer
- Authorised Pharmaceuticals Manufacturing Activities of the Site
- Any Other Manufacturing activities carried out on the site
- Quality Management System of Manufacturer
- The Quality Management System of Manufacturer
- Release Procedure of finished products
- Management of suppliers and Contractors
- Quality Risk Management (QRM)
- Product Quality Reviews
- Personnel
- Premises and Equipment
- Premises
- Equipment
- Documentation
- Type of Products
- Process Validation
- Material Management and Warehousing
- Production
- Quality Control (QC)
- Distribution, Complaints, Product Defects and Recalls
- Self-Inspection
Countries in PIC/S
• Argentina | • Denmark | • Poland | • Sweden |
• Australia | • Estonia | • Portugal | • Switzerland |
• Austria | • Finland | • Romania | • Thailand |
• Belgium | • France | • Singapore | • Turkey |
• Canada | • Malta | • Slovak Republic | • Spain |
• Chinese Taipei | • Mexico | • Norway | • Ukraine |
• Croatia | • Netherlands | • Slovenia | • United Kingdom |
• Cyprus | • New Zealand | • South Africa | • U.S.A |
• Czech Republic | • Norway | • Spain |