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Pharmaceutical Analysis Track

Ensuring Patient Safety through Analytical Control of Impurities Across Modalities: Panel Discussion

Tuesday, July 15, 2025
11:05 AM - 11:55 AM ET
Location: Vienna Ballroom: North
Pharmaceutical Analysis Track
This panel discussion will explore the critical role of analytical control of impurities in ensuring patient safety across diverse drug modalities. Panelists will discuss the latest regulatory guidelines and analytical techniques used to identify and control impurities in small molecules, biologics, and advanced therapies. Attendees will gain valuable insights into the challenges and innovative strategies for managing impurities in drug substances, complex generics, and emerging modalities such as antibody-drug conjugates (ADCs). Experts will also share practical approaches to controlling extractables and leachables (E&L), elemental impurities, and chiral characterization, all aimed at ensuring regulatory compliance and improving drug safety and efficacy.

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