On-Demand Webinar: An Introduction to Medical Device Regulation

By Engaged Expert Lisa Ferrara

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Lisa Ferrara, Ph.D., Technical Director for Element’s Medical Device Consulting and Regulatory Division, presents an introduction to the FDA's regulatory process for regulating medical devices, hosted by Medical Product Outsourcing.

The regulatory pathways for multiple classifications of medical devices are discussed, along with an overview of the process to take a new device from concept to commercialization and the associated challenges.

To learn more about the regulatory process and the challenges to receiving final approval for your medical device, please fill out the form below.

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