Real-World FDA Regulatory Strategies for Medical Device Software, Upcoming Webinar Hosted by Xtalks


Join this webinar and dive into The FDA regulations for healthcare software products, covering strategy, pathways and clinical data expectations.

Join Connie Qiu, MEng, RAC, Senior Consultant, Regulatory Affairs, ProPharma MedTech, for the live webinar on Wednesday, December 6, 2023, at 10am EST (4pm CET/EU-Central).

For more information, or to register for this event, visit Navigating SaMD and SiMD: Real-World FDA Regulatory Strategies for Medical Device Software.

ABOUT XTALKS

Xtalks, powered by Honeycomb Worldwide Inc., is a leading provider of educational webinars and digital content to the global life science, food, healthcare and medical device communities. Every year, thousands of industry practitioners (from pharmaceutical, biotechnology, food, healthcare and medical device companies, private & academic research institutions, healthcare centers, etc.) turn to Xtalks for access to quality content. Xtalks helps professionals stay current with industry developments, regulations and jobs. Xtalks webinars also provide perspectives on key issues from top industry thought leaders and service providers.

To learn more about Xtalks visit http://xtalks.com
For information about hosting a webinar visit http://xtalks.com/why-host-a-webinar/

Media Contact

Vera Kovacevic, Xtalks, +1 (416) 977-6555 x371, [email protected]

SOURCE Xtalks

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