Following are the useful articles on quality control management and analysis those are helpful to new as well as the experienced pharmaceutical professionals in quality improvement of products .This page is updated on a regular basis, therefore, don’t forget to visit again.
- Operating and Calibration of Total Organic Carbon Analyzer
- Standard Operating Procedure for Handling of Hazardous & Poisonous Chemicals
- Standard Operating Procedure For House Keeping
- Standard Operating Procedure for Sampling of Packaging Materials
- Standard Operating Procedure For Cleaning of Laboratory Glass wares
- Standard Operating Procedure For Laboratory Safety
- Resampling & Retesting of Materials
- Rinse Water Analysis
- Spares & Accessories of Instruments
- Maintenance of QC Equipments
- Procedure to Work Under Fume Hood
- Determination of Manufacturing Date for QC chemicals
- Indenting, Purchasing, Receiving, Storage & Issuance of QC chemicals
- Operation of Reverse Laminar Air Flow
- Shelf Life of Chemicals and Reagents
- Operation of Digimatic Micrometer
- Receipt, Issuance, Performance, Regeneration, Use, Cleaning, Storage and Rejection of GC Columns
- Operation and Calibration of Autotitrator & K F Titrator
- Operation and Calibration of Polarimeter
- Operation and Calibration of Viscometer
- Operation and Calibration of Photofluorometer
- Operation and Calibration of Bursting Strength Tester
- Operation and Calibration of Vacuum Oven
- Operation of Milli-Q-Water System
- Cleaning, Operation and Calibration procedure of Friability tester
- Operation and Calibration of Tap Density Test Apparatus
- Operation of Vernier Caliper
- Operation of Magnetic Stirrer
- Operation of Vacuum Pump
- Operation of Pin Hole apparatus
- Operation and calibration of Moisture Meter
- Calibration of Volumetric Apparatus
- Cleaning and operation of Sieve Shaker
- Handling of Pantone Colour Guide Booklet
- Operation and Calibration of Mini Rotary Shaker RS 12 Plus
- ANALYTICAL METHOD VERIFICATION PROTOCOL FOR RESIDUAL SOLVENT OF SILDENAFIL CITRATE Ph. Eur.
- ANALYTICAL METHOD VERIFICATION PROTOCOL FOR ASSAY OF SILDENAFIL CITRATE Ph. Eur
- ANALYTICAL METHOD VERIFICATION PROTOCOL OF RELATED SUBSTANCES OF SILDENAFIL CITRATE Ph. Eur.
- ANALYTICAL METHOD VERIFICATION PROTOCOL FOR IMPURITY E (BY TLC) OF SILDENAFIL CITRATE Ph. Eur.
- ANALYTICAL METHOD VERIFICATION PROTOCOL OF ASSAY OF NAPROXEN 500 MG TABLETS
- ANALYTICAL METHOD VERIFICATION PROTOCOL FOR RESIDUAL SOLVENT OF NAPROXEN Ph. Eur.
- ANALYTICAL METHOD VERIFICATION PROTOCOL FOR RELATED SUBSTANCES OF NAPROXEN Ph. Eur.
- ANALYTICAL METHOD VERIFICATION PROTOCOL OF ENANTIOMERIC PURITY OF NAPROXEN Ph. Eur.
- ANALYTICAL METHOD VERIFICATION PROTOCOL FOR ASSAY OF NAPROXEN Ph. Eur.
- ANALYTICAL METHOD VERIFICATION PROTOCOL FOR RELATED SUBSTANCE OF ERYTHROMIN 250 MG GASTRO-RESISTANT TABLETS
- ANALYTICAL METHOD VERIFICATION PROTOCOL FOR DISSOLUTION OF ERYTHROMYCIN 250 MG GASTRO-RESISTANT TABLETS
- ANALYTICAL METHOD VERIFICATION PROTOCOL FOR CONTENT UNIFORMITY OF ERYTHROMYCIN 250 MG GASTRO-RESISTANT TABLETS
- ANALYTICAL METHOD VERIFICATION PROTOCOL FOR ASSAY OF ERYTHROMYCIN 250 MG GASTRO-RESISTANT TABLETS
- ANALYTICAL METHOD VERIFICATION PROTOCOL FOR IDENTIFICATION BY TLC OF ERYTHROMYCIN Ph. Eur.
- ANALYTICAL METHOD VERIFICATION PROTOCOL FOR RESIDUAL SOLVENT OF ERYTHROMYCIN Ph. Eur.
- ANALYTICAL METHOD VERIFICATION PROTOCOL OF RELATED SUBSTANCES OF ERYTHROMYCIN Ph. Eur.
- ANALYTICAL METHOD VERIFICATION PROTOCOL FOR ASSAY OF ERYTHROMYCIN Ph. Eur.
- RESUDIAL SOLVENT METHOD VERIFICATION PROTOCOL OF CETIRIZINE DIHYDROCHLORIDE Ph. Eur.
- RELATED SUBSTANCES METHOD VERIFICATION PROTOCOL OF DICLOFENAC SODIUM BP
- METHOD VERIFICATION PROTOCOL FOR ASSAY FOR DICLOFENAC SODIUM BP
- METHOD VERIFICATION PROTOCOL FOR ASSAY OF CITALOPRAM HYDROBROMIDE Ph. Eur.
- MULTIMEDIA DISSOLUTION PROTOCOL OF CITALOPRAM 20 MG AND 40 MG TABLETS
- PROTOCOL FOR VALIDATION OF METHOD OF ANALYSIS FOR CLEANING SAMPLE OF CITALOPRAM TABLETS
- ANALYTICAL METHOD VERIFICATION PROTOCOL OF ASSAY OF CHLORPHENAMINE 4MG TABLETS
- RESIDUAL SOLVENT METHOD VERIFICATION PROTOCOL OF CHLORPHENAMINE MALEATE Ph.Eur.
- RELATED SUBSTANCES METHOD VERIFICATION PROTOCOL OF CHLORPHENAMINE MALEATE
- Cleaning of Platinum/Silica Crucibles
- Backup,Archival,Restoration and Challenge Test of Electronic Data
- METHOD VERIFICATION PROTOCOL FOR ASSAY OF CHLORPHENAMINE MALEATE Ph. Eur.
- ANALYTICAL METHOD VALIDATION PROTOCOL FOR RELATED SUBSTANCES OF CETIRIZINE DIHYDROCHLORIDE TABLETS
- DISSOLUTION PROFILING STUDY PROTOCOL OF CETIRIZINE DIHYDROCHLORIDE TABLETS
- ANALYTICAL METHOD VALIDATION PROTOCOL OF DISSOLUTION OF CETIRIZINE DIHYDROCHLORIDE TABLETS
- ANALYTICAL METHOD VALIDATION PROTOCOL OF ASSAY AND CONTENT UNIFORMITY OF CETIRIZINE DIHYDROCHLORIDE TABLETS
- VALIDATION OF SPREADSHEET CONTROL AND ACCURACY OF RESULT
- ASSAY METHOD VALIDATION PROTOCOL OF TRYPSIN – CHYMOTRYPSIN TABLETS
- METHOD VERIFICATION PROTOCOL FOR DETERMINATION OF RESIDUALSOLVENT IN SILDENAFIL CITRATE
- RELATED SUBSTANCES METHOD VALIDATION PROTOCOL OF SILDENAFIL CITRATE TABLETS
- ANALYTICAL METHOD VALIDATION PROTOCOL FOR DISSOLUTION METHOD OF SILDENAFIL CITRATE TABLETS 50 mg
- METHOD VALIDATION PROTOCOL FOR DETERMINATION OF RESIDUAL SOLVENT IN CITALOPRAM HYDROBROMIDE
- ANALYTICAL METHOD VALIDATION PROTOCOL FOR THE DETERMINATION OF N-METHYL-3-PYRROLIDINOL IN GLYCOPYRRONIUM BROMIDE BY GAS CHROMATOGRAPHY
- PERFORMANCE QUALIFICATION DOCUMENT OF GC WITH HEAD SPACE ON CHROMELEON SOFTWARE
- ASSAY METHOD VERIFICATION PROTOCOL OF OFLOXACIN TABLETS
- DISSOLUTION METHOD VERIFICATION PROTOCOL OF OFLOXACIN TABLET
- ASSAY METHOD VALIDATION PROTOCOL OF Ofloxacin and Ornidazole Tablets
- ASSAY METHOD VALIDATION PROTOCOL OF SILDENAFIL CITRATE TABLET IP
- DISMANTLING VERIFICATION DOCUMENT FOR QC INSTRUMENT
- PROTOCOL FOR VALIDATION OF METHOD OF ANALYSIS FOR CONTAMINATION STUDY OF PARACETAMOL
- PROTOCOL FOR VALIDATION OF METHOD OF ANALYSIS OF CLEANING SAMPLE OF PARACETAMOL 325 mg AND DICLOFENAC SODIUM 50 mg TABLET
- PROTOCOL FOR VALIDATION OF METHOD OF ANALYSIS FOR CLEANING SAMPLE OF ONDANSETRON TABLET
- PROTOCOL FOR VALIDATION OF METHOD OF ANALYSIS FOR CLEANING SAMPLE OF CITALOPRAM HYDROBROMIDE TABLET
- PROTOCOL FOR CLEANING METHOD VALIDATION OF IBUPROFEN 100MG & PARACETAMOL162.5MG SUSPENSION/5ML FOR IBUPROFEN
- RELATED SUBSTANCES METHOD VALIDATION PROTOCOL FOR CITALOPRAM TABLET
- ASSAY METHOD VALIDATION PROTOCOL FOR CITALOPRAM HYDROBROMIDE
- RELATED SUBSTANCES METHOD VERIFICATIN PROTOCOL FOR CITALOPRAM HYDROBROMIDE
- DISSOLUTION METHOD VALIDATION PROTOCOL FOR CITALOPRAM TABLETS
- ASSAY METHOD VALIDATION PROTOCOL FOR CALCIUM & VITAMIN D3 TABLETS
- SOP For Out of Calibration (OOC) of Laboratory Instruments
- INSTALATION, OPERATIONAL AND PERFORMANCE QUALIFICATION DOCUMENT OF DISSOLUTION APPARATUS
- Standard Operating Procedure For Sampling of Packaging Materials
- Trend Analysis of Out of Specification Results
- Standard Operating Procedure of Analytical Method Transfer
- Analytical Method Technology Transfer
- Analytical Method Validation For Equipment Wash Water Samples
- Operation and Calibration of BOD Incubator
- Microbiological Analysis of Purified Water, Pretreatment Water and Source Water