Share this postLet's Talk Risk!Quick Tip: Integrate clinical evaluation activities in your product development plan. Copy linkFacebookEmailNotesMoreQuick Tip: Integrate clinical evaluation activities in your product development plan. Insight from a conversation with Sarah PantenNaveen Agarwal, Ph.D.Feb 12, 2024Share this postLet's Talk Risk!Quick Tip: Integrate clinical evaluation activities in your product development plan. Copy linkFacebookEmailNotesMoreShareListen to the full podcast hereLTR 24: Clinical evaluation is a lifecycle process, not a one-time activityNaveen Agarwal, Ph.D.·October 6, 2023The current medical device regulation in the European Union (EU-MDR) includes the term clinical evaluation more than 140 times! Clearly, clinical evaluation is now more important than ever under EU-MDR (and IVDR). As a result, a general feeling in the medical device industry is that it is now significantly more challenging to bring innovative new devices…Read full storyThank you for reading Let's Talk Risk!. This post is public so feel free to share it.SharePreviousNext