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Development of Medicinal Products with Co-Packaged Devices/Cross-Referenced Devices: Challenges and Opportunities
Session Chair(s)
Andreas Emmendoerffer, DrMed, PhD
Regulatory Group Director - Device and Combination Products
Roche, Switzerland
This session will explore the development of medicinal products with co-packaged devices/cross-referenced devices, its challenges and the opportunities that arise with it. The session will start with scene-setting presentations that serve as a foundation for parallel roundtable discussions, encouraging in-depth collaborative discussions in smaller groups focused on solutions and strategies.
Speaker(s)
Christelle Bouygues, PharmD
European Medicines Agency, Netherlands
Regulatory Affairs Senior Officer
Isabelle Mingam
UCB, Switzerland
Associate Director, Global Regulatory Affairs CMC and Medical Devices
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