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Regulatory 2.0

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The Regulatory 2.0 track is a two-day intensive program that will prepare leaders in medtech to manage through the evolving landscape at the FDA and abroad with the new EU-MDR.

Changes in regulatory landscape have a material impact on how biologics, drugs and medical devices get to market, this course will bring you up to speed on everything you need to know about what is evolving in the global regulator landscape. Day One will concentrate on changes domestically at the FDA and Day Two will feature an immersive curriculum on everything you need to know about how the new EU MDR will impact our industry. This content is brought to you by experts at R&Q.