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Additive Manufacturing and the FDA

Wyss EventLecture

In this talk, Dr. Di Prima will discuss his role as a regulatory scientist in the CDRH at the FDA and will be providing a high-level summary of medical device regulations and submission types. The FDA’s history with additively manufactured medical devices will then be covered along with the FDA’s regulatory approach for these products. Dr. Di Prima will also be providing a summary of some of the ongoing FDA additive manufacturing research projects.

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