SOP
- STABILITY STUDY PROTOCOL
- SOP on the Transfer of Technology for Analytical Method
- Why disinfectant sterilization required in pharma injectable?
- 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
- OOS in Microbiology
- Deviation Handling and Quality Risk Management As Per WHO
- 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)
- Calibration of KARL FISCHER (METTLER TOLEDO)
- Calibration procedure for friability test apparatus
- 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 SAS SUPER 100 AIR SAMPLER
- Humidity Chamber
- 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
- Approval of vendors (Packing Materials)
- Vendor Development and Approval (API and excipients)
- CLEANING VALIDATION FOR DRUG PRODUCTS
- The role of dissolution in drug development
- Procedure for operation of Autotitrator (METTLER TOLEDO). Quality assurance
- PROCEDURE FOR OPERATION OF HUMIDITY CONTROL OVEN (NEWTRONIC)
- Types of Glass used in Pharmaceutical Industries
- PROCEDURE FOR MICROBIOLOGICAL MONITORING OF WATER
- RAW MATERIAL PRE-SAMPLING INSPECTION CHECKLIST BY QUALITY CONTROL ANALYST
- Qualification For Stability Chamber ( STABILITY DATA ACQUSITION SOFTWARE)
- DISINFECTANT VALIDATION
- PROTOCOL TO EVALUATE EFFICACY OF UV GERMICIDAL LAMP WITH KNOWN MICROORGANISM
- Unit Dose Sampling Procedure for Blend Uniformity
- Worst case identification for cleaning validation
- VALIDATION MASTER PLAN
- MANAGEMENT REVIEW OF QUALITY METRICS
- Temperature Mapping
- Types of liquid column chromatography( HPLC)
- SOP for environmental monitoring of air
- Procedure for calibration of balance XS 204 DR.
- Deviation Handling and Quality Risk Management (Part – I)
- Question and Answer on Cleaning validation in Pharmaceutical Industry
- Master Plan or Protocol for Process Capability Design and Testing
- 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
- 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)
- Preparation of Validation and Qualification Protocols
- SOP on Quality Risk Management
- 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
- 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
- SOP on New Product Design and Development Process
- SOP On In-process Control of Packing Line
- SOP on Sampling of Intermediates and Finished Products
- SOP On In-process Control During tablets Manufacturing
- SOP on Line Clearances
- SOP ON PRODUCT RECALL AND MOCK RECALL PROCEDURE
- Sop on Corrective and Preventive Action (CAPA)
- Sop on Recording of Specimen Signature
- HANDLING AND MANAGEMENT OF PRODUCT COMPLAINT
- HANDLING OF CHANGE CONTROL
- Assigning Manufacturing and Expiry date
- SOP Template: Operating Standard Procedure
- Standard Operating Procedure – How to Create an SOPs Effective
- SOP ON SOP-STANDARD OPERATING PROCEDURE/GENERAL TEST PROCEDURES
- Product Quality Review (PQR) SOP
- Handling of Deviations SOP
- Cleaning Policy of Area & Equipment SOP
- Good Documentation Practices SOP
- SOP FOR TEMPLATE FOR PROCESS VALIDATION PROTOCOL IN PHARMA