In this free webinar, learn about developing regulatory strategies for medical devices with software components. Attendees will get a comparison of US regulatory landscapes and pathways to market. The featured speaker will discuss clinical data expectations, algorithm validation and training. Attendees will hear considerations for developing regulated software medical device products and real-world examples of applied strategies.
TORONTO, Nov. 20, 2023 /PRNewswire-PRWeb/ -- Administration (FDA) regulations for healthcare software products, and explore regulatory strategies, pathways to market and clinical data expectations. Software products are used in a variety of healthcare applications including tracking personal health and well-being, monitoring vital signs, administering therapies, facilitating diagnoses and treatment decisions and aiding with surgical procedures.
This webinar will discuss how to determine whether a software function and/or product meets the definition of a medical device, software as a medical device (SaMD) or software in a medical device (SiMD), that is subject to The FDA regulatory oversight. Potential pathways for bringing these software products to market will be explored along with points to consider in developing short and long-term regulatory strategies. The expert speaker will also discuss how algorithm training and validation and clinical data expectations may be impacted by the selected regulatory pathway.
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.
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