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DeviceTalks West 2017 has ended
Monday, December 11 • 2:30pm - 3:30pm
The regulatory pathway of tomorrow: How do we gameplan for changes in Silver Springs, EMEA and more?

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Changes at the FDA and its foreign counterparts could alter the way medical technology gets to market. After years of increasing predictability for device companies, what will create more uncertainty in the coming years? A panel of experts from across the industry discuss how best to game plan for changes in Silver Springs and beyond. 

Moderators
avatar for Theresa  Miles

Theresa Miles

Directory of Client Solutions, Regulatory and Quality Solutions (R&Q)

Speakers
avatar for Daniel Beard

Daniel Beard

Promenade Software
avatar for Theresa  Miles

Theresa Miles

Directory of Client Solutions, Regulatory and Quality Solutions (R&Q)
avatar for Frank Pokrop

Frank Pokrop

Director, Regulatory Affairs, Becton Dickinson
Frank is a Director of Regulatory Affairs at Becton Dickinson in San Diego – formerly CareFusion.  He is a member of ASQ, ISACA and RAPS and holds these certifications:   RAC, CSQE, CISA and CPGP.  Frank is also the president of the San Diego Regulatory Affairs Network (SDRAN... Read More →
avatar for Chip Zimliki

Chip Zimliki

Regulatory Affairs, Medtronic Diabetes
Charles Zimliki, Ph.D. is Sr. Director of Regulatory Affairs for the Intensive Insulin Management Business Unit within Medtronic Diabetes.  He is responsible for communicating with FDA on behalf of insulin pumps, continuous glucose monitors, and closed-loop device systems including... Read More →


Monday December 11, 2017 2:30pm - 3:30pm
TBA

Attendees (14)