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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 on a June 6 webinar at http://medgroup.biz/standards 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 at http://medgroup.biz/standards 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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June 14 webinar: Why Your Data Needs to be in the GDSN (Global Data Synchronization Network)

Government agencies in the US, UK, EU and elsewhere now are mandating electronic product data submissions. And major customers including Group Purchasing Organizations and hospital networks need access to the data in a standard format.

You need to know about the GDSN. Join us at http://medgroup.biz/GDSN

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Make it a great week.

Joe Hage
Medical Devices Group Leader

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Emma Xie
Manager
We also have many Customers from all over the world, and don’t know how to manage it.