Quality Assurance
- Interview Questions & Answers (Quality Assurance)
- Observations & Compliances response of GMP Inspections
- ANVISA – The Brazilian Health Surveillance Agency
- New Product Design and Development Process
- Technical Directions for Drug Product Manufacturing
- Un-Planned Deviation -3 in Pharma
- Un-Planned Deviation -II in Pharma
- Un-Planned Deviation in Pharma
- SOP LIST (Quality Assurance)
- List of SOPs Quality Control
- Organization and Personnel in Pharma industry as per USFDA
- Document Management System in Quality Assurance Department in Pharma Industry
- Management Review
- SOP on SOP in Industry (Pharmaceuticals Industry)
- Line Clearance
- Indian Pharmacopoeia Commission (IPC)
- 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 FOR DRUG PRODUCTS
- PROCEDURE FOR MICROBIOLOGICAL MONITORING OF WATER
- Unit Dose Sampling Procedure for Blend Uniformity
- Worst case identification for cleaning validation
- VALIDATION MASTER PLAN
- MANAGEMENT REVIEW OF QUALITY METRICS
- Temperature Mapping
- Deviation Handling and Quality Risk Management (Part – I)