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Pharmaceutical analysis - An overview of the latest possibilities of using GC a GCMS systems 2019-2020

Th, 3.12.2020
| Original article from: LabRulezGCMS Library/Pharma & Biopharma
Overview of applications, presentations, technical articles, posters or practical manuals using GC and GCMS systems from 2019 - 2020 in the field of pharmaceutical analysis.
Pixabay/Mizianitka: 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

Search in more than 7,000 GC and GCMS documents in the LabRulezGCMS database.
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