What To Expect From FDA’s New Approach to Regulate Medical Software
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Deadline: December 17, 2019 | Date: December 17, 2019
Venue/Country: U.S.A
Updated: 2019-11-04 21:39:08 (GMT+9)
Call For Papers - CFP
The FDA’s emerging approach to medical software product regulation has important ramifications for patients, healthcare providers and insurers as well as product developers. So, it is critically important for companies throughout the life sciences and healthcare industries that utilize software in its products to understand the important challenges and opportunities presented by this major policy shift. This webinar will provide understanding.Keywords: Accepted papers list. Acceptance Rate. EI Compendex. Engineering Index. ISTP index. ISI index. Impact Factor.
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