Join this webinar to gain insights into:
- The comparison of the regulatory landscapes for medical devices and IVDs in the EU and US
- Risk classification of medical devices and IVDs in the EU and US and its impact on product development and associated requirements
- How to develop a rigorous clinical and regulatory plan to support your priority market
- Guidance on aligning product development and go-to-market strategies
- Real-world examples that bring these key considerations to life
Join Matthew Nowland, Vice President, Regulatory Affairs, MedTech, Premier Consulting; and Michael Edwards, Senior Director, Regulatory Affairs, MedTech, Premier Consulting, for the live webinar on Friday, November 3, 2023, at 11am EDT (4pm CET/EU-Central).
For more information, or to register for this event, visit Medical Device Development and Market Strategy: Europe or US First? Or Both?
ABOUT XTALKS
Xtalks, powered by Honeycomb Worldwide Inc., is a leading provider of educational webinars to the global life science, food and medical device community. Every year, thousands of industry practitioners (from life science, food and medical device companies, private & academic research institutions, healthcare centers, etc.) turn to Xtalks for access to quality content. Xtalks helps Life Science professionals stay current with industry developments, trends and regulations. Xtalks webinars also provide perspectives on key issues from top industry thought leaders and service providers.
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Vera Kovacevic, Xtalks, +1 (416) 977-6555 x371, vkovacevic@xtalks.com
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