Quality Assurance
- All Post URL of Drugs formulations
- SOP on SOP
- QUALITY SYSTEMS MODEL IN PHARMACEUTICAL INDUSTRY (Part – I)
- CGMPS AND THE CONCEPTS OF MODERN QUALITY SYSTEMS
- What are good documentation practices & how can they best be implemented?
- Drug Master Files (DMFs) and it submission
- Quality Assurances SOPs List
- Pharmaceutical Quality Assurance -Drug and Therapeutics Committee Training Course
- PPT on prevent the spread of COVID 19 infection at the workplace
- USFDA GUIDELINE FOR DRUG QUALITY SAMPLING AND TESTING (DQST)- HUMAN DRUGS
- List of Documents required for Quality Assurance Departments (GMP Compliances)
- In-process control of oral drug product during manufacturing & Packing
- PROCEDURE FOR OPERATION OF UNIT DOSAGE SAMPLER
- Batch Release Statement for Pharmaceutical Product
- SOP In-process Control of Packing Lines
- SOP on Sampling of Intermediates and Finished Products
- SOP On In-process Control During Tablets Manufacturing
- SOP on Line Clearance
- SOP on QUALITY RISK MANAGEMENT (RISK ASSESSMENT)
- SOP on the Transfer of Technology for Analytical Method
- SOP on Transfer of Technology for Manufacturing process
- Technology transfer
- Correction of Documentation Errors
- New Product Design and Development Process
- Approval of vendors (Packing Materials)
- Vendor Development and Approval (API and excipients)
- Cleaning validation in pharmaceuticals
- PROCEDURE FOR MICROBIOLOGICAL MONITORING OF WATER
- Unit Dose Sampling Procedure for Blend Uniformity
- Worst case identification for cleaning validation
- VALIDATION MASTER PLAN
- Management Review
- Temperature Mapping
- Deviation Handling and Quality Risk Management (Part – I)
- 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”).
