Join Marc Chaillou and Peter Muller who have more than 15 years of experience in labeling and compliance as they reflect on how the industry has transformed, and where it’s headed next. From increasing regulatory complexity and globalization to the shift from manual, explore the major changes that have shaped labeling over the past decade and a half. Through real-world insights, lessons learned, and practical tips, attendees will gain a deeper understanding of the operational and regulatory shifts impacting labeling today, as well as emerging technologies from authoring and review platforms to AI-supported compliance solutions, that are redefining the future of labeling while keeping humans at the center of decision-making.
Learning Objectives
- Learn historical background for regulatory affairs professionals & practical information for what’s coming next.
- Understand how organizations have evolved from manual processes to digital labeling and compliance workflows.
- Explore how emerging technologies, including AI, are influencing the future of labeling while maintaining human oversight.
Who Should Attend?
- Pharmaceuticals and Medical Device
- Regulatory Affairs Professionals
- Labeling and Artwork Specialists for Pharma and Medical Device
- Medical And Technical Writers
- Teams Involved in Epi
Audience Learning Level
Basic: Content is introductory in nature and requires no requisite knowledge or experience to grasp concepts and related exercises. Basic educational activities are meant to establish a foundation of knowledge and/or competence that will be expanded upon in practice or in higher level activities.
Proof of Attendance
A certificate of attendance can be downloaded from the RAPS Learning Portal following the event.
Questions
Contact the RAPS Support Center:
Call +1 301 770 2920, ext. 200 (8:30 am–5:30 pm EST, Monday–Friday) or email [email protected]
Peter Muller
Marc Chaillou
