Falls Church, VA (PRWEB) March 05, 2015
Understanding China’s New Medical Device Regulations
**FDAnews Webinar**
March 26, 2015 — 1:30 p.m. – 3:00 p.m. EDT
http://www.fdanews.com/UnderstandingChinaMDRegs
There has been an explosion of new and revamped regulations for medical devices in China.
These new regulations touch on all aspects of medical devices — research and development, approval, manufacturing, distribution, and post-market surveillance. And they affect all devices — those currently in development as well as those that are already on the market.
John Balzano, a foremost authority on U.S. and China medical device regulations will cover how the new China rules for devices will be implemented, and address major concerns in detail, including:
Attendees will come away from this 90-minute session understanding how the new regulations will affect operations in China … the problems companies are already encountering with the new regulations … and how they’re solving those problems.
Meet the Presenter:
John Balzano is special counsel in the New York office of Covington and Burling, LLP and practices in the firm’s food and drug group. Mr. Balzano represents companies and industry associations on U.S. and China regulatory and policy matters in the drug, biologic, medical device (including in vitro diagnostics), cosmetic and food spaces. He assists companies with compliance with the regulations of the China Food and Drug Administration (CFDA) and the National Health and Family Planning Commission (NHFPC) and advises on how to develop strategies for bringing their products to market in China.
Who Will Benefit:
Conference Details:
Understanding China’s New Medical Device Regulations
**FDAnews Webinar**
March 26, 2015 — 1:30 p.m. – 3:00 p.m. EDT
http://www.fdanews.com/UnderstandingChinaMDRegs
Tuition:
$287 per site
Easy Ways to Register:
Online: http://www.fdanews.com/UnderstandingChinaMDRegs
By phone: 888-838-5578 or 703-538-7600
About FDAnews:
FDAnews is the premier provider of domestic and international regulatory, legislative, and business news and information for executives in industries regulated by the US FDA and the European Medicines Agency. Pharmaceutical and medical device professionals rely on FDAnews' print and electronic newsletters, books and conferences to stay in compliance with international standards and the FDA's complex and ever-changing regulations.
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