Join us for an insightful webinar designed to highlight the benefits you can gain from partnering with a top-tier Contract Development and Manufacturing Organization (CDMO). Discover how our advanced Antibody-Drug Conjugate (ADC) platform enables you to develop processes and manufacture a diverse range of novel conjugates to meet your specific drug development needs. We will highlight the advantages of focusing on Process Analytical Technology (PAT) and how its strategic integration into our development workflows enhances our technical capabilities. Learn how our commitment to PAT not only accelerates process development but also ensures the delivery of high-quality products from the start.
In this webinar, you will learn:
- How to leverage a robust ADC platform to scale-up and manufacture multiple novel conjugates
- Incorporation of Process Analytical Technology (PAT), can deepen process understanding and results in better data collection in fewer development runs
- Utilization of PAT has led to faster, more efficient process development strengthening our First-Time-Right philosophy
Speakers

Melissa Ritchie
MilliporeSigma
Senior Scientist, Analytical Development
Melissa joined MilliporeSigma's process and analytical development team in 2018. She started her career as a fellow scientist at ORIS and FDA DPA and was a postdoc fellow at UNC Chapel Hill. With a strong background in protein biochemistry and bioconjungation, she has more than seven years of experience in the industry. Melissa holds a Ph.D. from the Wake Forest School of Medicine.

Sowmyan Sreenivasaraghavan
MilliporeSigma
Scientist, ADC Process Development
Sowmyan joined MilliporeSigma's process and analytical development team in 2019. Before his current role, he optimized mAb downstream processes within the MSAT operations and developed novel processes for dairy proteins and lipids. He has eight years of experience in industrial biotech and food science. Sowmyan holds an M.S. from the Ohio State University.
Pharma and biopharma manufacturing
- Pharma and biopharma manufacturing
Duration:1h
Language:English
Session 1:Thu, May 15, 2025 5:00 PM CEST
To continue reading please sign in or create an account.
Don't Have An Account?