SOP
- SOP on Procedure for microbiological monitoring of Purified water in pharmaceutical company
- SOP on Procedure for viable air monitoring 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 Sampling of raw materials in pharmaceutical company
- SOP on Samping of packing materials in Pharmaceutical company
- SOP on Procedure for cleaning and storage of sampling devices
- 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
- SOP on Operating procedure for halogen moisture balance
- SOP on Operating procedure for leak test apparatus in pharmaceutical company
- SOP on Operating procedure for vernier caliper in Pharmaceutical company
- SOP on Procedure for operation of HPLC (waters-alliance)
- SOP on Procedure for operation of analytical balance
- SOP on Operating procedure for tap density apparatus make : electrolab
- SOP on Operating procedure for sieve shaker in quality control
- Procedure for calibration of Instruments/ Equipments.Quality Assurance
- SOP On Installation, Operational and Performance qualification of Equipment
- Preparation, Approval and Control of Standard Cleaning Procedures for equipments
- SOP On Document and Data Control
- SOP ON SOP (Standard Operating Procedures)
- Process Validation: General Principles and Practices (January 2011)
- Stability Testing
- STABILITY STUDY
- Preparation of Validation and Qualification Protocols
- Pharmaceuticals Facility and cGMP Expectations
- SOP on Quality Risk Management
- SOP on Acceptable Quality Level (AQL) During Product Inspection for physical defects.
- SOP on Artwork Design and Approval
- SOP on writing & approval of Qualification and validation protocol & reports
- SOP on Maintaining of Equipment Log Book
- SOP On Issuance and Submission of Batch Manufacturing Record (BMR)
- SOP on Recording of Specimen Signature
- Preparation, Approval, Review and Control of MFC and MPC for Manufacture of Pharmaceutical Products
- CALIBRATION PROCEDURE FOR HALOGEN MOISTURE ANALYSER
- Collection, Storage and Control of Control Samples for Drug Products
- Responsibilities of Quality Assurance Department
- In-process checks during Packaging Operation of tablets and capsules
- Numbering System for Qualification Documents, Protocols and Reports
- Installation, Operational and Performance qualification of Equipment/Instrument.
- Vendor Development, Qualification, De-qualification and Requalification for Raw Materials & Packing Material
- Release of Finished Products
- Review of Batch Manufacturing Record
- Basic Requirement of Documentation and Records for GMP Compliance
- SOP on New Product Design and Development Process
- SOP On In-process Control of Packing Line
- SOP on Sampling of Intermediates and Finished Products