Manufacturing, QA/QC - Related Information

Analysis of Impurities in Alcohol-Based Hand Sanitizers by GC-MS [ PDF / 476.15KB ]

Efficient Analysis of Residual Solvents in Pharmaceuticals Using the Compact Model, Brevis GC-2050 (2) - JP18 and USP467, Water Insoluble Samples [ PDF / 431.77KB ]

Efficient Analysis of Residual Solvents in Pharmaceuticals Using the Compact Model, Brevis GC-2050 (1) - JP18 and USP467, Water-Soluble Samples [ PDF / 583.15KB ]

TOC Evaluation of Ammonia Solution [ PDF / 607.48KB ]

Strength Evaluation of Pharmaceuticals and PTP Packaging [ PDF / 569.16KB ]

LC-MS/MS Method for Detection and Quantitation of Azido Impurities in Irbesartan Drug Substance [ PDF / 313.35KB ]

Quantitation of NDMA and NDEA in Metformin and 5 SartanAPIs as per the EDQM method Procedure B [ PDF / 215.06KB ]

Quantitative analysis of azido impurity in the sartandrugs using LC-MS/MS [ PDF / 527.72KB ]

Determination of Epichlorohydrin from Sevelamer carbonate as per proposed USP monograph GC method [ PDF / 289.63KB ]

Quantitation of Varenicline Nitroso-Drug Substance Related Impurity (VNDSRI) in Varenicline API by GC-MS/MS [ PDF / 267.73KB ]

Determination of Organic Impurities from Valproic Acid as per proposed USP monograph GC method [ PDF / 356.53KB ]

Flame Photometric Analysis of Sodium in Lithium Carbonate Using Wavelength Shift Function of AA-7800 [ PDF / 321.9KB ]

Contaminant Analysis of Pharmaceuticals (Tablets) Using AIRsight Infrared/Raman Microscope [ PDF / 382.32KB ]

Seamless Purification for Drug Discovery with Screening, Preparative, and Purity check [ PDF / 1.8MB ]

Spectral Transmission Measurement of Pharmaceutical Containers [ PDF / 325.3KB ]

Simultaneous Analysis of 10 Nitrosamines in an Active Pharmaceutical Ingredient Using a Triple Quadrupole Mass Spectrometer [ PDF / 318.68KB ]

Simultaneous Analysis for Drug Purity Test and Quantitative Assay [ PDF / 878.25KB ]

Identification Testing of Myo-Inositol Conforming to the European Pharmacopoeia (EP) [ PDF / 490.89KB ]

Qualitative Determination of Abietic Acid Improperly Used in Prepared Chinese Medicines [ PDF / 697.58KB ]

Analysis of Elemental Impurities in Mediumchain Triglycerides According to USP [ PDF / 734.5KB ]

Residual Solvents Analysis in Pharmaceuticals by HS-GC-FID with Newly Added Compounds –USP Procedure A [ PDF / 173.02KB ]

Organic Impurity analysis of Levofloxacin Drug Material following USP monograph [ PDF / 212.88KB ]

Analysis of Voglibose by Post-Column Derivatization Method [ PDF / 510.42KB ]

Determination of Dexamethasone and its organic impurities content as per USP monograph UHPLC method [ PDF / 497.97KB ]

Determination of Ticagrelor and its related impurities content from oral tablets as per proposed IP monograph UHPLC method [ PDF / 515.54KB ]

Analysis of Extractables from Pharmaceutical Packaging Materials by Solvent Extraction-GCMS and Headspace-GC-MS [ PDF / 336.49KB ]

Packed Column Analysis of Alcohol Number Determination Conforming to Japanese Pharmacopoeia Using Nexis™ GC-2030 (FID) [ PDF / 343.34KB ]

Analysis of Sodium Chondroitin Sulfate by ELSD-LT III [ PDF / 131.97KB ]

Analysis of Volatile Impurities in Anhydrous Ethanol and Ethanol for Disinfection in Accordance with the Purity Test set by the Pharmacopoeias (JP, USP, EP) - Gas Chromatography [ PDF / 235.38KB ]

Measurement of Impurities in Ethanol Using UV-Vis Spectrophotometer - Spectrophotometric Analysis [ PDF / 307.46KB ]

USP-Compliant Analysis of Vitamin in Dietary Supplement : Analysis of Cyanocobalamin by Nexera™ XR - High Performance Liquid Chromatography [ PDF / 101.17KB ]

USP-Compliant Analysis of Vitamins in Dietary Supplements Analysis of Calcium Pantothenate by Nexera™ XR - High Performance Liquid Chromatography [ PDF / 83.24KB ]

Analysis of Purified Glucose and Glucose Hydrate in Accordance with the Japanese Pharmacopoeia - High Performance Liquid Chromatography [ PDF / 86.73KB ]

Ultraviolet-Visible Spectrophotometry Under JP/EP - Use of Evaluation Function of LabSolutionsTM UV-Vis [ PDF / 115.55KB ]

Instrumental Validation of UV-Visible Spectrophotometer Compliant with JP, EP and USP – Application of Instrumental Validation Functions of UV-1900 – [ PDF / 1.12MB ]

A Goal-Oriented Approach to the Quantitative Determination of Cannabinoids by HPLC - Pittcon 2017 1130-12 [ PDF / 434.07KB ]

Application of Online SFE-SFC-PDA for Cleaning Validation [ PDF / 1MB ]

Analysis of Omeprazole by "i-Series" for USP and JP Methods [ PDF / 918.62KB ]

Analysis of Mannitol Using RID-20A Differential Index Detector [ PDF / 847.18KB ]

Introduction of Performance Validation Software for Improved GLP/GMP Support - Spectrophotometric Analysis [ PDF / 1.45MB ]

Analysis of Ethanol and Anhydrous Ethanol in Accordance with the Fifteenth Edition of the Japanese Pharmacopoeia - SPECTROPHOTOMETRIC ANALYSIS [ PDF / 77.9KB ]

Analysis of Colored Components on the Surface of Tablets - SPECTROPHOTOMETRIC ANALYSIS [ PDF / 120.89KB ]

Organic Impurity Analysis of Cetirizine Hydrochloride Drug Material Following USP Monograph [ PDF / 282.88KB ]

TOC Analysis for Purified Water, Water for Injection and Clean-In-Place Applications - System Suitability Test [ PDF / 71.68KB ]