Quality Assurance
- Question and Answer on Cleaning validation in Pharmaceutical Industry
- Code to Code Transfer of Materials and Additional Testing of Materials / Products
- CALIBRATION MASTER PLAN
- SOP on In-process sampling of semi-finished product
- SOP on execution of exhibit batches
- SOP on withdrawal, storage, observation & destruction of control/retention sample
- SOP on preparation, control, issuance and revision of Batch Manufacturing and Batch Packing Records
- SOP on line clearance
- SOP on Monitoring of Temperature, Relative Humidity and Pressure Differential
- SOP on Technology Transfer for Analytical Method
- SOP on Transfer of Technology for Manufacturing process
- SOP on Execution of Exhibit Batches
- SOP for Sampling of In-process blends, uncoated tablets, coated tablets and filled capsules
- SOP on Training
- SOP on Drug Product Recalls
- Issuance and Evaluation of Product Exception Investigation Reports (“EIRs”).
- SOP on Process Validation Programmed in Pharmaceutical Company
- Preparation, Approval, Issue and Control of Art works for labeling of Pharmaceutical products
- Calibration for Weighing Balances
- Calibration procedure for halogen moisture analyzer
- Handling of Returned Pharmaceutical Products
- SOP for calibration of disintegration test apparatus
- Procedure for calibration of calculator
- Change Control Review SOP
- Change Control in Pharma Industries
- HANDLING OF MARKET COMPLAINTS
- SOP For Control of Completed Batch Production
- Review of Batch Production Records
- SOP For Release of Finished Products
- SOP For Process Area clearance during batch/product changeover
- SOP For Assigning of repacking before date
- SOP on Cleaning of Sampling Aids
- SOP on Annual Product Review of Drug Product Quality (APQR)
- SOP on Cleaning Validation in pharmaceutical company
- Reporting, Investigating and Disposition of Incidents
- Cleaning of Unit Dose and Large Volume Sampling Thieves
- Responsibilities of Quality Assurance Department
- Collection, Storage and Control of Reserve Samples for Drug Products
- Correction of Documentation Errors
- In-process checks during Packaging Operation of tablets and capsules
- Assigning of expiry date to a finished product
- Technical training and evaluation of Quality Assurance Officers.
- SOP on In-process control of packing Process in Pharmaceutical company
- SOP on In-process control during tablet manufacturing in Pharmaceutical company
- SOP on Sampling of intermediates and finished products in pharmaceutical company
- Procedure for line clearances. Quality assurance
- SOP on Procedure for operation and cleaning of unit dosage sampler
- SOP on Handling of Out of Specification Results in quality control
- SOP on Operating procedure for disintegration test apparatus in Pharmaceutical company
- SOP on Operating procedure for friability test appratus