September 18-20, 2018
Tuesday, September 18th, 2018, 2:30 PM EST | 11:30 AM PST
Thursday, September 20th, 2018, 8:30 AM EST | 1:30 PM GMT | 2:30 PM CET
Duration: 30 mins
If you are responsible for method development and optimization, impurity detection and characterization, and problem-solving in support of pharmaceutical development and manufacturing, this webinar is for you.
Pharmaceutical process development involves multi-disciplinary groups, with analysts responsible for ensuring product safety through putting in place, effective impurity control measures. While mountains of analytical and chemical data are generated (LC/MS, HPLC, data, synthetic routes, reagents, starting materials, reaction conditions etc.) each functional team has its own specific challenges based on their contributions to the process.
In the second webinar of this two-part series we will focus on how impurity data management software (Luminata) supports the analytical chemist's workflow.
If you are also interested in learning how synthetic route information can be managed effectively in Luminata, read more about Part I in this Webinar Series.
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Join us in this webinar to see how you can:
In addition to all this, we will share stories from real users about the productivity gains they have made and how the software has contributed to efficiency while eliminating tedious, manual calculations and data transfer.