Regulatory Affairs 2018-05-22T19:50:15+00:00
Pre-Proposal Applications for Interdisciplinary Translation Program due July 27, 2018.  Please click here for more information.

Regulatory Affairs


The MPWRM Resource Center’s regulatory experts are available to provide regulatory guidance for medical devices, biologics and combination products. Our experienced subject matter experts can advise on strategy at all stages of new product development and post-marketing activities, and preparing applications for FDA’s review.

Contact Patrick Cantini at cantinip@upmc.edu for more information about the regulatory services available or to be connected to one of our regulatory consultants for guidance.

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