Thursday (Nov. 18) join the Office of Innovation and Economic Development for a workshop on regulatory pathways for medical devices. This session will cover essential principles and practices for anyone working on or considering medical device development. Learn about the critical regulations specific to medical devices, identify key stakeholders and resources, and get help navigating the regulatory process from pre-market to post-market for any medical device.
Speaker: Danielle Parker, regulatory affairs manager at Baxter International
Parker, a UMaine alumna, has more than a decade of clinical and regulatory affairs experience.
Thursday, Nov. 18, 4–5:30 p.m. via Zoom.
For more info and registration, click here.
