List of Standard Operating Procedures (SOPs) in Quality Assurance : Pharmaceutical Guidelines

List of Standard Operating Procedures (SOPs) in Quality Assurance

List of GMP Standard operating procedures ( SOP ) for Quality Assurance system and procedures for pharmaceutical industry.

2. - Issuance of batch manufacturing record
3. - Change Control System
4. - Product Recall
5. - Deviation Procedure
6. - Reserve Samples (Retention Samples)
7. - Preparation of Working Reference Standards
8. - Periodic Observation of Control Sample
9. - Sampling Procedure For Packing Material
10. - Guidelines for the Investigation In Case of Final Product Rejection
11. - Sampling of Raw Material
12. - Self Inspection Programme
13. - Handling Of Customer Complaint
14. - Handling of Returned goods
15. - Destruction of Packing Material
16. - Disposal of Containers Containing Hazardous Material
17. - Sampling and Analytical Procedure For Wash Water
18. - Sampling Procedure For In process and Finished Product for QC Analysis.
19. - Vendor Selection and Approval
20. - Vendor Audit
21. - Operation of Laboratory Safety
22. - Detection of Foreign Particles
23. - Cleaning of Laboratory glass ware
24. - Batch Manufacturing Record (BMR) Control Procedure
25. - Replacing Damaged Batch Manufacturing Record (BMR)
26. - Cleaning of Sampling Devices
27. - Final Inspection and Release of Finished goods
28. - IPQC during Packaging Operation
29. - Validation Master Plan
30. - Process Validation
31. - Periodic Product Quality Evaluation of Marketed Products
32. - Quality Assurance Approval of Manufacturing Batch
33. - Periodic Review of standard operating procedure
34. - Release of Raw material coming from group Company
35. - For Testing of Residual Solvents or Organic Volatile Impurities In Raw Material coming from group Company.
36. - Preparation and handling of Buffers, Indicator, Colorometric   solution, Limit standard solution, volumetric solutions and reagents
37. - IPQC during compression operation
38. - For Testing of Residual Solvents or Organic Volatile Impurities In Raw Material coming from Other than group Company.

Ankur Choudhary is India's first professional pharmaceutical blogger, author and founder of Pharmaceutical Guidelines, a widely-read pharmaceutical blog since 2008. Sign-up for the free email updates for your daily dose of pharmaceutical tips.
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