Webinar: Reduce your time investment in impurity data management
Posted: 16 June 2020 | ACD/Labs | No comments yet
Pharmaceutical process development involves multi-disciplinary groups of chemists and analysts whose goal it is to create the API by the cheapest, most efficient route while ensuring product safety through effective impurity control measures.
A vast amount of analytical and chemical data is generated (LC/MS, HPLC, data, synthetic routes, reagents, starting materials, reaction conditions etc.) and is managed in many different systems, not necessarily designed to handle this data, and requires huge manual effort by the scientists.
Watch this webinar to see how you can:
- Centralise and assemble all your analytical and chemical process information in one informatics platform and reduce tedious, time-consuming data transcription
- Collaborate effortlessly with team members and track impurities in real-time
- Search and access impurity data more easily to establish effective controls faster
Intended Audience:
VP/Director Process Development
VP/Director Analytical Development
Process chemists and scale-up chemists
API development teams
Analytical development and process analytical chemists
Development project team leaders
Regulatory affairs
Related topics
Active Pharmaceutical Ingredient (API), Analytical techniques, HPLC, Impurities, Liquid Chromatography - Mass Spectrometry (LC-MS)
