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Understanding FDA Design Verification and Validation Requirements for Medical Devices

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Deadline: February 12, 2019 | Date: February 12, 2019

Venue/Country: U.S.A

Updated: 2019-01-12 01:29:58 (GMT+9)

Call For Papers - CFP

This webinar will help you understand specific product verification and validation requirements for medical devices to comply with ISO 13485: 2016 and FDA quality system regulations. It will focus on the topics such as product development process, traceability and risk management at all stages, design outputs and documentation in DMR and DHR, design verification and design validation activity cycles and more.

Keywords: Accepted papers list. Acceptance Rate. EI Compendex. Engineering Index. ISTP index. ISI index. Impact Factor.
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