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Submissions

Digital Design Control for Medical Devices

Medical Device companies have to manage complexity and regulation without placing excess overhead on their designers. Devices complexity has led to increased complaints, CAPAs, observations, and recalls. The root cause is frequently insufficient and cumbersome design control. Digitalization helps them design with agility while maintaining control. It improves speed, accuracy, and productivity by automating submissions,…

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Jim Brown - February 20, 2018 - Filed Under: Presentations & Video, Tech-Clarity TV, Video - Tagged With: Digital Design, Medical Device, Digital Design Control, Traceability, Submissions, Compliance, vlog, Observations, Tech-Clarity TV, Digitalization, Recalls, Video, Product Innovation Platform, Innovation, Design History File, Siemens PLM, DHF, Quality, FDA, CAPA, Med Device, Device Master Record, Digital Enterprise, DMR

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