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It’s happening: 2020 is here and we are mere months away from the official European Union Medical Device Regulations (MDR) May 26 date of application. The corrigenda didn’t get us out of it and no additional delays are coming - even with COVID-19 at our heels - so by this time you should be well into your EU MDR transition and familiarized with the new regulations.

Whether the upcoming deadline is a cause for comfort or grief – don’t panic! Compliance is possible and our online workshop will get you access to industry and R&Q experts who are familiar with the hurdles your organization is facing. In this workshop you can get your questions answered and stay ahead of the deadlines.

RA/QA leaders from multinational medical device companies – along with preeminent RA/QA experts from R&Q – will share strategic solutions for challenging problems that we have seen so far. You will have the opportunity to ask questions throughout the workshop and will leave with an advanced skillset and developed strategies no matter where you are in the EU MDR transition process.

Click the button below to learn more, see the agenda, and register for FREE.

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We are passionate about your success. Tell us more about your regulatory and quality needs to learn about how we can help.

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