USP 467 - Residual Solvent Application Updates - Tips & Tricks
Drug manufacturers have to ensure that the impurities are removed or are present only in limited concentration for toxicological concerns.
The acceptable level of residual solvents has been established by the ICH. USP have implemented a new test requirement for the control of residual solvents in drug products.
To know latest trends & workflow Solution, attend exclusive webinar on Accurate & reproducible resulits using Agilent's latest Residual Solvent analysis workflow.
You would be updated with:
- Systematic approach in conducting Residual Solvent analysis.
- Analytica Workflow & System Solutions to get accurate & reproducible results.
- Tips & tricks for getting best outcomes in your day to day analysis.
Presenter: Soma Dasgupta (Application Specialist GC and GC/MS, Agilent Technologies)
She brings over 15 years of research experience with gas chromatography allowing her to explore many aspects of this analytical technique to solve questions across different sectors ranging from food safety to pharmaceuticals. Prior to joining Agilent Technologies, she performed her doctorate research at the University of Pune where she concentrated on developing comprehensive methods for analysis of agro-chemicals in fruits and vegetables. She has worked with Thermo Fisher Scientific for 3 yrs as Application specialist. On joining Agilent, she became part of a team responsible for developing solutions to meet customers' analytical needs. She specialize in multi-residue method development; pesticides and environmental applications and genotoxic impurities in pharmaceuticals. She has more than 25 publications and application notes to her credit and a book chapter.
