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Countdown to MD&M West 2013: Eleven Days until the Most Comprehensive MedTech Conference in the Nation
Date:1/31/2013

ANAHEIM, California, January 31, 2013 /PRNewswire/ --

More than 500 high-level MedTech professionals in all functions, and from all over the world, will convene at the 2013 MD&M West Conference.  MD&M West is one of the most anticipated face-to-face gatherings for those involved in medical device design and manufacturing. The four-day Conference takes place Feb. 11-14, 2013 at the Anaheim Convention Center. To reserve your space, visit http://www.MDMWestConference.com.

     (Logo: http://photos.prnewswire.com/prnh/20130131/593901)

The 2013 Conference will host six FDA/CDRH (Center for Devices and Radiological Health) officials, who will be speaking on timely medical device industry topics:

Randall Brockman
Acting Chief Medical Officer, Office of Device Evaluation, FDA/CDRH

Topic: FDASIA Recap: Clarifying the review process and the benefit-risk determinations for PMA and de novo applications

Don St. Pierre

Deputy Director for New Product Evaluation, Office of In Vitro Diagnostic Device Evaluation & Safety, FDA/CDRH

Topic: Reviewing the 510(k) Triage and Quick Review pilot program and an update on the new process, including the RTA policy change

Alonza Cruse
District Director, FDA Los Angeles District

Topic: FDA Los Angeles District Update and the FDA Globalization Initiative

Dan Solis
Director of Import Operations, FDA Los Angeles District

Topic: Update on Los Angeles Import Operations Activities

Ron Kaye
Team Leader; Human Factors Pre-Market Evaluation Team, Office of Device Evaluation, FDA/CDRH

Topic: Hu
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SOURCE UBM Canon
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