Expanding Opportunities

Webinar: Navigating AI Compliance in Life Sciences: FDA Policy Insights for AI Governance Discover how to harness AI in life sciences without compromising compliance. In this webinar, FDA AI policy expert Danielle Dorfman Faruq and Renee VonBergen explore AI governance, data integrity, human oversight, transparency, monitoring, and validation. Gain practical strategies to implement compliant AI, strengthen quality processes, and build a scalable roadmap for successful AI adoption.

Join us for two Outsourced Pharma Capabilities Update sessions featuring leading CDMOs sharing their facilities, timelines, and available capacity for development and manufacturing. The April 21st session focuses on small molecule drug product capabilities, while April 22nd highlights fill-finish technologies including sterile filling, lyophilization, and advanced packaging. Expect short digital presentations to help biopharma companies identify partners that can meet their manufacturing needs.

Webinar: Extractables, Leachables, and Risk: Ensuring Safety in Pharma Manufacturing Join this expert-led Pace webinar to gain a clear, step-by-step strategy for managing extractables and leachables (E&L) risk. Discover how to assess materials, assign risk scores, and reduce testing burdens—all while staying aligned with USP requirements. Whether you're launching new products or prepping for regulatory submissions, this session will streamline your approach.