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Understanding China’s Medical Device Regulations
China has dramatically revamped its medical device regulations in every major area including:
And its equivalent of the FDA, the CFDA, isn’t close to being finished with ticketing advertising and promotion, adverse event reporting, and device classification for new regulation this year.
John Balzano, a leading authority on U.S. and China medical device regulation, will break it all down for you in one 90-minute webinar CD and transcript. You’ll come away with a practical understanding of:
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.
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