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Webinar: Reduce your time investment in impurity data management

Posted: 16 June 2020 | | 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











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This content is provided to you for free thanks to the kind support of our sponsor: ACD/Labs

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