BioArbor: Cleared For Launch: Planning To Ensure Your Medical Product Is Approved

ANN ARBOR – Please join BioArbor for a presentation and Q&A with two US Food & Drug Administration regulatory experts on March 11 at Ann Arbor SPARK.

The program will cover topics essential when planning for FDA approval of medical products, including drugs and devices. Special attention will be given to recent trends, and issues that are relevant for smaller companies.

Heather S. Rosecrans, U.S. Food & Drug Administration, Stephen Goldner, Regulatory Affairs Associates.

Date: Wednesday, March 11

Time: 5 p.m.- Networking; 6 p.m. �?? Program

Location: SPARK Central, 330 East Liberty, lower Level, Ann Arbor

Cost: FREE

Click Here to register.

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