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Supporting mutagenic impurity and degradant risk assessment using an in silico approach

We recently held our first webinar of 2023, ‘Supporting mutagenic impurity and degradant risk assessment using an in silico approach’. This free-to-attend webinar featured talks from Dr. Andreas Broehl, Laboratory Head at Bayer Pharmaceuticals, and Lhasa Limited Senior Scientist, Dr. Ash Ali. In this exciting virtual event, we explored how our in silico software solution Zeneth, can […]

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United States Pharmacopeia (USP) Workshop on Nitrosamine Impurities

We were excited to attend USP’s Workshop on Nitrosamine Impurities, organised by United States Pharmacopeia (USP) in collaboration with Indian Pharmaceutical Alliance (IPA). Lhasa Principal Scientist, David Ponting presented within the Toxicity Assessment session, his presentation was titled ‘Application of in silico tools (QSAR) to predict toxicity’.  

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Genotoxic Impurities in Pharmaceutical Industry

We were excited to attend the Genotoxic Impurities in Pharmaceutical Industry Hybrid Conference! Held in Barcelona, Spain on the 26th and 27th of January and online, the Genotoxic Impurities in Pharmaceutical Industry conference contained case studies from large and small pharmaceutical companies. Discover the latest technical insights and discuss rapidly advancing technologies in Toxicology &

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