Pharmaceutical Guidance Complete Pharma Solution
- Document Management System in Quality Assurance Department.
- Management Review
- SOP on Standard Operating Procedures
- SOP For Line Clearance
- All Post URL of Drugs formulations
- SOP on SOP
- QC SOPs List
- Quality Assurances SOPs List
- Pharmaguidances Whats App Groups
- SOP on Testing Efficacy of Disinfectants
- SOP on Personnel Qualification for Aseptic Processing and Sterility Testing Area
- SOP on Personnel Qualification for Aseptic Processing and Sterility Testing Area
- SOP on Viable Particle Monitoring of Drain Points– Sterile Product Manufacturing Facility
- SOP on calibration of pH meter
- Sampling and testing of Sterile surgical Gloves
- PROCEDURE FOR CALIBRATION OF REFRIGERATOR
- USFDA GUIDELINE FOR DRUG QUALITY SAMPLING AND TESTING (DQST)- HUMAN DRUGS
- List of Documents required for Quality Control Departments (GMP & GLP Compliances)
- List of Documents required for Quality Assurance Departments (GMP Compliances)
- In-process control of oral drug product during manufacturing & Packing
- SAMPLING OF PACKING MATERIALS
- PROCEDURE FOR OPERATION OF UNIT DOSAGE SAMPLER
- Batch Release Statement for Pharmaceutical Product
- Procedure for Microbiological Monitoring of Purified water
- Inprocess Control of Packing Lines
- Sampling of Intermediates and Finished Products
- Inprocess Control During Tablets Manufacturing
- SOP on Line Clearance
- SOP on the Transfer of Technology for Analytical Method
- SOP on Transfer of Technology for Manufacturing process
- SOP on Fogging of Microbiology Testing Areas
- SOP on cleaning and operating procedure of bursting strength tester
- Handling of Microbiological Data Deviation in Microbiology Laboratory
- Calibration procedure for tap density apparatus [Make- electro Lab]. Quality assurance
- Procedure for operation and calibration of IR Spectro Photometer (SHIMADZU). Quality assurance
- Procedure for calibration of conductivity meter (PICO). Quality Assurance
- Calibration of KARL FISCHER (METTLER TOLEDO). Quality assurance
- Calibration procedure for friability test apparatus. Quality assurance
- Calibration procedure for disintegration test apparatus (ED-2AL)
- Procedure for operation of weighing balance (Make: METTLER TOLEDO)
- Procedure for operation of pH / CONDUCTIVITY METTLER (PICO)
- Operating procedure for milli Q water system
- Procedure for operation of walk in humidity chamber (25ºC/60%RH)
- Operating procedure for ultrasonic bath
- Calibration procedure for gas chromatograph clarus 500 with head space (Perkin Elmer)
- Area clearance during batch/product change over in Pilot Production facility. Quality Assurance
- Preparation, Approval and Control of Guidelines (Quality Assurance)
- Technology transfer
- Correction of Documentation Errors
- New Product Design and Development Process
- All Post URL of Drugs formulations
- Pharmaguidances Whats App Groups
- Deviation Handling and Quality Risk Management
- PPT on prevent the spread of COVID 19 infection at the workplace
- Investigating Out-of-Specification
- Stability Testing
- Stability Study
- Presentation on Hold Time Study of OSD
- 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
- Pharmaguidances Whats App Groups
- 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