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Device Master Record

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: CAPA, Compliance, Design History File, Device Master Record, DHF, Digital Design, Digital Design Control, Digital Enterprise, Digitalization, DMR, FDA, Innovation, Med Device, Medical Device, Observations, Product Innovation Platform, Quality, Recalls, Siemens PLM, Submissions, Tech-Clarity TV, Traceability, Video, vlog

Servicing Medical Equipment – Safety First, Profit Not Optional

Insight from Tech-Clarity’s research Servicing Medical Devices: World Class Service Management for Medical Equipment. This report is intended to help medical device companies leverage lessons learned from other service-oriented industries, but points out distinct differences in the healthcare industry.

Jim Brown - January 20, 2010 - Filed Under: Clarity on PLM, Insights, Insights & Activity - Tagged With: Device Master Record, DMR, Equipment Service Management, ESM, Manufacturers, Medical Device, Medical Equipment, Service Lifecycle Management, Service Management, SLM

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