Pharmaceutical Industries Quality Assurance SOP’s
- PREPARATION, REVIEW, APPROVAL, DISTRIBUTION CONTROL, REVISION, RETRIEVAL AND DESTRUCTION OF STANDARD OPERATING PROCEDURE (SOP for SOP)
- Preparation of Site Master File – SOP
- Documentation – SOP
- Handling of Deviation – SOP
- Training SOP
- Change Control SOP
- Vendor Qualification SOP
- Self Inspection SOP
- Product Recall SOP
- Handling of Market Complaints SOP
- Allocation of Product Batch Number SOP
- Assigning Manufacturing and Expiry Date SOP
- Handling of Returned Goods SOP
- Out of Specification SOP
- Qualification of Equipment / Instrument / Utilities SOP
- Approval of Finished Goods SOP
- Cleaning Validation SOP
- Line Clearance SOP
- Annual Product Quality Review (APQR) SOP
- In Process Quality Assurance (IPQA) SOP
- Incident Management SOP
- Failure Investigation SOP
- Corrective Action and Preventive Action SOP
- Handling of Online Rejection SOP
- Stability Studies SOP
- Abbreviations SOP
- Sampling of Intermediate and Finished Product SOP
- Calibration By External Agency SOP
- Management of Batch Manufacturing Record and Batch Packing Record SOP
- Temperature Mapping SOP
- Reconciliation During Batch Manufacturing and Batch Packing SOP
- Quality Risk Management SOP
- Preparation of User Requirement Specification (URS) SOP
- Handling of Out Of Trend (OOT) SOP
- Specimen Signature SOP
- Allocating identification number to instrument / equipment / utility
- Rinse and Swab Sampling From Equipment’s Product Contact Surface SOP
