Join Europe’s leading pharmaceutical, medical device manufacturers and regulatory bodies to discover how to:
Navigate the complex regulatory landscape on a global level: as Biogen, Confinis, Lloyds Register, Johnson & Johnson and Sandoz share key information to help you understand and interpret regulatory guidelines
Develop a project raoadmap and end to end lifecycle management strategy by hearing how Sanofi and Johnson & Johnson have developed and launched successful combination products
Create an effective post market maintenance strategy by learning how Teva are managing the surveillance and maintenance of products throughout the entire lifecycle
Assess and manage risk and safety procedures by hearing two separate presentations from Biogen and Bayer that provide key process, strategy and steps you can apply as a standard approach across different combination products
Understand and interpret regulations, apply a human factors strategy and align drug-device departments by attending three separate interactive workshops led by expert facilitators that will help answer your unique questions
Download the agenda to view the full list of speakers and sessions >>
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