Managing Regulatory Standards in Multiple Jurisdictions
Organizations today are faced with a growing list of new and changing standards, and keeping pace with them has become increasingly difficult.
It’s hard enough to manage regulations in one country, much less multiple countries.
How are the most efficient medical device companies handling this challenge?
Join me and regulatory technology experts from Instem to learn how their approach is meeting this challenge and enabling clients of all shapes and sizes to more efficiently manage all global standards with complete confidence.
If you’re on a regulatory team and presently creating and managing registrations and submissions, this presentation is for you.
Instem’s guest speaker and a Global Regulatory Affairs expert will present an industry perspective on the current medical device challenges.
So if you’re operating in multiple countries, register now to learn how to more easily navigate through these complexities.
The main takeaway is this: You need an efficient and practical way to manage all of your device registration information amidst a changing regulatory (UDI, EU MDR, IDMP…) landscape.
We’ll record the call and get the slides to you, even if you can’t make the live event.
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