Webcast Replay
Taking Advantage of the EU MDR Delay in Uncertain Times – Optimizing Your Medical Device RA/QA Strategy
The life science regulatory landscape in Europe is evolving quickly and irrevocably. These changes are anticipated to strengthen the regulatory platform and to slowly drift apart from the siloed approach practiced by device manufacturers and related organizations in the EU.
In this RAPS webinar, you will have an opportunity to develop a comprehensive, and advanced understanding of the potential strategic solutions for EU MDR compliance, regardless of where you are in the transition process.
Additionally, you will also learn how to proactively take advantage of the extension for both MDD renewal and MDR implementation to effectively manage every facet of the regulatory change.
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If you’re curious how Celegence can help improve your Regulatory Operations then contact us now to arrange a meeting!