Join us for an insightful and practical webinar on “Navigating AI Adoption in GMP-Regulated Areas While Staying Compliant.”
Key Insights:
- AI in Pharma Production: Explore how AI is revolutionizing pharmaceutical production through process automation, real-time quality control, predictive maintenance, and AI-driven batch release decisions.
- Regulatory Perspectives: Gain insights into how regulators in the U.S. and the EU are approaching AI in GMP-compliant manufacturing, focusing on validation, risk management, and compliance expectations.
- Broader Frameworks: Understand how AI adoption fits into broader regulatory frameworks like the EU AI Act.
Featured Speakers:
- Gert Thurau, Lead Technology Innovation Manufacturing, CMC Regulatory Policy, Roche
- James Johnson, Partner, Sidley
- Jay Jariwala, Senior Director, Regulatory Compliance, Sidley
- Eva von Mühlenen, Senior Advisor, Sidley
Why Attend?
This session will provide a real-world discussion on how companies can effectively integrate AI into their operations while adhering to Good Manufacturing Practice (GMP) regulations.
Learn from industry and regulatory thought leaders about the latest trends and best practices in AI adoption within GMP-regulated environments.
Who Should Attend?
Executives, in-house counsel, quality and compliance managers and officers interested in and/or facing GMP compliance and quality management challenges in Switzerland.
For more information or questions, please contact gvaevents@sidley.com.
Nothing in this program may be quoted or used in any manner without the express written consent of Sidley Austin LLP. The views expressed in this program are the views of the participants, and not necessarily those of the firm. This program is for informational purposes only and should not be considered legal advice or creating an attorney-client relationship.
