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EU Medical Device Regulatory Affairs Conference
October 1, 2023 All day
The EU Medical Device Regulatory Affairs Conference is suited to audiences of regulatory affairs, compliance and legal, clinical affairs, medical affairs, manufacturing operations, engineering and testing, sales, marketing and reimbursement, training and education and information technology.
Attendees can expect to optimise their regulatory oversight with perspectives from notified bodies and industry peers. At the conference, speakers will exchange practical methods to strengthen regulatory strategy, best practices for communicating with notified bodies and lessons learned in receiving approval with limited guidance.
Attendees can expect to learn how to Improve patient outcomes and internal operations by gaining methods to achieve sufficient data for successful product submissions. Attendees can customize their experience and address their unique concerns during dynamic Q&A after each session.
Why attend?
- Learn from industry leaders
- Keep up with industry trends
- Exchange ideas and network
- Find solutions that work for you
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