Pharmaceutical analysis - An overview of the latest possibilities of using GC a GCMS systems 2019-2020
Pixabay/Mizianitka: Pharmaceutical analysis - An overview of the latest possibilities of using GC a GCMS systems 2019-2020
Take a look at the latest trends in drug production analysis using gas chromatographs (GC), headspace autosamplers (HS), GC/MS, GC/QQQ, or the combination of gas chromatography with high resolution mass spectrometers (HRMS).
The latest technologies push the boundaries of detection limits in all application areas - from the analysis of residual solvents, through today's critical analyzes of nitrosamines to the analysis of extractable and leachable substances from packaging materials.
Thanks to the possibilities of our unique database with advanced search, you are able to search and filter in a second according to the exact configuration of the system, manufacturer or industries.
All documents directly available in LabRulezGCMS database.
GC/HRMS (2)
Analytical solutions for challenges in headspace GC-MS analysis of volatile extractable and leachable compounds |2019| Thermo Fischer Scientific
Extractables & LeachablesAnalysis of Pharmaceutical Nasal Spray Samples using the Hi-Resolution Accurate Mass GC/QTOF |2019| Agilent Technologies
GC/QQQ (7)
Combined Direct Injection N-Nitrosodimethylamine (NDMA),N-Nitrosodiethylamine (NDEA), N-Nitrosoethylisopropylamine (NEIPA), N-Nitrosodiisopropylamine (NDIPA), and N-Nitrosodibutylamine (NDBA)Impurity Assay by GC-MS/MS | 2019 | Ostatní
Analysis of Five Nitrosamine Impurities in Drug Products and Drug Substances Using Agilent GC/MS/MS Instrumentation | 2020 | Agilent Technologies
Analysis of Pharmaceuticals’ Impurity - Regulations and Analysis for Carcinogenic Substances | 2020 | Shimadzu
Nitrosamine Impurities Application Guide - Confidently Detect and Quantify Mutagenic Impurities in APIs and Drug Products | 2020 | Agilent Technologies
Quantification of Nitrosamine Impurities in Metformin Using Agilent GC/MS/MS Instrumentation | 2020 | Agilent Technologies
Overcoming the challenges of nitrosamine impurities in drugs | 2020 | Thermo Fischer Scientific
Determination of 33 pesticide residues in Ginseng using gas chromatography-triple quadrupole mass spektrometry | 2020 | Shimadzu
GC/SQ (12)
Determination of genotoxic nitrosamines in Valsartan with gas chromatography and mass spektrometry | 2019 | Thermo Fischer Scientific
Analysis of N-Nitrosodimethylamine and N-Nitrosodiethylamine Using the Agilent 7697A Headspace Sampler, 8890/5977 GC/MSD Systém | 2019 | Agilent Technologies
Analysis of USP <467> Residual Solvents of Class 1, Class 2, and Class 3 using the Agilent 8890 GC/ FID /5977B MSD Systém | 2019 | Agilent Technologies
Selective and Sensitive Analysis of 20 Category I and II Residual Solvents for Cannabis Application using Headspace-GCMS | 2020 | Shimadzu
Analysis of Terpene and Terpenoid Content in Cannabis Sativa Using Headspace with GC/MSD | 2020 | Agilent Technologies
Analysis of NDMA and NDEA in Sartan Drugs and Drug Products by GC-MS on a Zebron™ ZB-624PLUS™ | 2019 | Phenomenex
Agilent ASMS 2020 Posters Book | 2020 | Agilent Technologies
Analysis of Pharmaceuticals’ Impurity - Regulations and Analysis for Carcinogenic Substances | 2020 | Shimadzu
Nitrosamine Impurities Application Guide - Confidently Detect and Quantify Mutagenic Impurities in APIs and Drug Products | 2020 | Agilent Technologies
Overcoming the challenges of nitrosamine impurities in drugs | 2020 | Thermo Fischer Scientific
Thermal Desorption – GCMS Method for Screening Analysis of Extractables in Drug Packaging Materials | 2020 | Shimadzu
GC (15)
Analysis of Residual Solvents in Pharmaceuticals An Analysis Method for Class 2 Solvents (Water- Soluble Samples) Unsuited to Headspace GC Methods | 2019 | Shimadzu
Analytical solutions for challenges in headspace GC-MS analysis of volatile extractable and leachable compounds | 2019 | Thermo Fischer Scientific
Analysis of USP Method <467> Residual Solvents on the Agilent 8890 GC System | 2019 | Agilent Technologies
Analysis of USP <467> Residual Solvents of Class 1, Class 2, and Class 3 using the Agilent 8890 GC/ FID /5977B MSD System | 2019 | Agilent Technologies
Enhanced Productivity for Residual Solvent Analysis in Pharmaceutical Products According to USP 467 by Using a New Valve and Loop Static Headspace Sampler | 2019 | Thermo Fischer Scientific
Investigation of Key Parameters for a Smooth Method Transfer to a New Optimized Valve and Loop Headspace Autosampler | 2019 | Thermo Fischer Scientific
Investigation of key parameters for a smooth method transfer to the new Thermo Scientific TriPlus 500 Headspace Autosampler | 2019 | Thermo Fischer Scientific
System Suitability Test of Low-Substituted Hydroxypropyl Cellulose for USP42-NF37 | 2020 | Shimadzu
Analysis of Residual Solvents in Pharmaceuticals by Nexis™ GC-2030 + HS-20 (JP17 Supplement II, USP 467) | 2020 | Shimadzu
Analysis of Residual Solvents in Pharmaceuticals by Water-Soluble Samples Using N2 Carrier (JP17 Supplement II, USP 467) | 2020 | Shimadzu
Analysis of Residual Solvents in Pharmaceuticals by Water-Insoluble Samples Using N2 Carrier (JP17 Supplement II, USP 467) | 2020 | Shimadzu
Analysis of Volatile Impurities in Anhydrous Ethanol and Ethanol for Disinfection in Accordance with the Purity Test set by the Pharmacopoeias (JP, USP, EP) | 2020 | Shimadzu
Alcohol Determination of Sanitizer Gel in accordance with USP<611> | 2020 | Shimadzu
Analysis of Residual Solvents in Pharmaceutical Products by Headspace-GC-FID with Nitrogen Carrier Gas Following USP<467> - Procedure B | 2020 | Shimadzu
Packed Column Analysis of Alcohol Number Determination Conforming to Japanese Pharmacopoeia Using Nexis™ GC-2030 (FID) | 2020 | Shimadzu