Pharmaceutical Guidance Complete Pharma Solution
- Total Organic Carbon in Water in Pharma Industry
- Analytical Method Validation protocol
- CLINICAL TRIAL PROTOCOL
- All Post URL of Drugs formulations
- UV LAMP EFFICACY TEST
- UV efficacy Challenge test
- Cleaning Validation – Glossary of Terms
- 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
- Pharmaceutical Quality Assurance -Drug and Therapeutics Committee Training Course
- STABILITY STUDY PROTOCOL
- Why disinfectant sterilization required in pharma injectable?
- The role of dissolution in drug development
- Types of Glass used in Pharmaceutical Industries
- RAW MATERIAL PRE-SAMPLING INSPECTION CHECKLIST BY QUALITY CONTROL ANALYST
- Qualification For Walk In Chamber ( STABILITY DATA ACQUSITION SOFTWARE)
- PROTOCOL TO EVALUATE EFFICACY OF UV GERMICIDAL LAMP WITH KNOWN MICROORGANISM
- VALIDATION MASTER PLAN
- Types of liquid column chromatography ( HPLC),HPLC Separation and HPLC Silica gel
- Deviation Handling and Quality Risk Management (Part – I)
- Master Plan or Protocol for Process Capability Design and Testing
- QUALITY BY DESIGN (QBD) IN PHAARMACEUTICAL PRODUCT
- Process Validation: General Principles and Practices (January 2011)
- Pharmaceuticals Facility and cGMP Expectations
- Basic Requirement of Documentation and Records for GMP Compliance
- SOP On Document and Data Control
- Annexure – III For SOP on SOP
- Annexure – II For SOP on SOP
- Annexure – 1For SOP on SOP
- Annexure – I for Anual product quality Review