C4C Event Oct 4: Medical Device and Diagnostics – Early Regulatory Product with a Product in Mind

Bringing a product to market in a regulated area can be challenging. Early planning can smooth the path to and through the FDA, and help you make the most of limited dollars.

Join us to learn more about what to expect in filing for regulatory approval and how best to design your bench studies with that goal in mind. Presenters Mike Maloney and Kirk Van Ness have 50+ years of wide-ranging regulatory experience in medical device and diagnostics. Bring your questions, and expect lots of case studies.

DATE: Thursday, Oct 4, 2012, 10:00 to 11:00 am

LOCATION: Fluke Hall, 3rd Floor presentation space

SPEAKERS: Michael Maloney, RAC, Executive Vice President of Development and Regulatory Services, Intertox &
Kirk Van Ness, Ph.D. DABT, Senior Toxicologist at Intertox

Please RSVP to Valerie Carricaburu by Oct 1, 2012