Published by
@ShahidNShah
@ShahidNShah
August 2 to August 5, 2021
It is an online event.
This 4-day course will navigate the 510(K) clearance process and De Novo classifications requests for the United States (U.S.) and Global Medical Device Manufacturers and regulatory affairs leaders to improve the ability to bring new and improved devices to the U.S. marketplace.
Continue reading at us-tdm-tso-15eb63ff4c6-1626e-169df4b0a12.force.com
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