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Case for Quality

Medical Device Manufacturers’ Software

Medical Device Manufacturers’ Software Selection Guide (buyer’s guide)

What should you think about when selecting a software solution to support the development of medical devices while considering the Case for Quality and the EU MDR? Tech-Clarity’s Medical Device Manufacturers’ Software Selection Guide helps manufacturers identify the right buying criteria for software solutions to support developing, producing, and servicing medical devices. The guide also…

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Michelle Boucher - April 17, 2020 - Filed Under: Buyer's Guides, Published Research - Tagged With: 3D Printing, ALM, AR, Augmented Reality, Buyer's Guide, CAPA, Case for Quality, Compliance, Criteria, Embedded Software, EU MDR, FDA, Healthcare, Internet of Things, IoT, ISO 13485, Medical Design Regulation, Medical Device, NPD, PLM, Product Development, Quality Management, Regulations, Requirements, UDI

Medical Devices

Medical Devices Manufacturers Software Selection Guide for 2018

Thank you for your interest in the Medical Devices Manufacturers Software Selection Guide for 2018  Buyer’s Guide! Please enjoy complimentary access from our sponsor, PTC. Tech-Clarity’s Medical Devices Manufacturers Software Selection Guide for 2018 helps manufacturers identify the right buying criteria for software solutions to support developing, producing, and servicing medical devices. For 2018, the guide has…

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Jim Brown - October 31, 2018 - Filed Under: Hidden - Tagged With: ALM, Buyer's Guide, CAPA, Case for Quality, Compliance, Criteria, Embedded Software, FDA, Healthcare, Internet of Things, IoT, ISO 13485, Medical Device, NPD, PLM, Product Development, Quality Management, Regulations, Requirements, UDI

Translating Digital Buzzwords to Real Value for Medical Devices (post)

Tech-Clarity research shows that the majority of manufacturers believe that digitalization is important or critical to achieving their business strategy (see figure). Over one-third say that it’s critical. Digitalization in medical device design and manufacturing has significant promise, but what does it actually mean? Medical device companies, already struggling with how to address critical initiatives…

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Jim Brown - October 1, 2018 - Filed Under: In the News - Tagged With: Analytics. EU MDR, Case for Quality, DHF, Digital Enterprise, Digital Thread, Digital Twin, Digitalization, DMR, IIoT, IoT, Life Sciences, Medical Device, Production Twin

Medical Devices

Medical Devices Manufacturers Software Selection Guide for 2018

Tech-Clarity’s Medical Devices Manufacturers Software Selection Guide for 2018 helps manufacturers identify the right buying criteria for software solutions to support developing, producing, and servicing medical devices. For 2018, the guide has also been updated to include additional considerations for the Internet of Things (IoT). This buyer’s guide also takes into account unique needs for medical device…

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Michelle Boucher - January 30, 2018 - Filed Under: Buyer's Guides, Published Research - Tagged With: ALM, Buyer's Guide, CAPA, Case for Quality, Compliance, Criteria, Embedded Software, FDA, Healthcare, Internet of Things, IoT, ISO 13485, Medical Device, NPD, PLM, Product Development, Quality Management, Regulations, Requirements, UDI

Medical Devices

Medical Devices in a Digital World (podcast)

Listen to Michelle Boucher discuss trends in the Medical Device Industry in this 17 minute podcast, Medical Devices in a Digital World. This podcast is episode 8 of The Connected Engineer series with Gavin Quinlan. In this episode, Michelle explains some of the top challenges facing medical device companies. She also shares advice on how to overcome them….

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Michelle Boucher - October 19, 2017 - Filed Under: Presentations & Video - Tagged With: Case for Quality, Compliance, Cost of Compliance, Engineer, FDA, IoT, Medical Device, PLM, Podcast, PTC, Regulation, Smart Connected Products, Traceability

Medical_Device_Novartis

Live Interview – Achieve the Case for Quality (webcast)

Hear Michelle Boucher’s interview with David Wolf from PTC on medical devices. They focused on key topics for medical device companies, including the Case for Quality. During the discussion, Michelle shared research on medical device industry trends. She also discussed the implications for the Case for Quality and offered advice to efficiently manage regulatory compliance. Throughout the discussion, she asked David…

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Michelle Boucher - June 6, 2017 - Filed Under: Presentations & Video, Webinars - Tagged With: Case for Quality, Compliance, Design, Engineer, FDA, IEEE, Medical Device, PTC, Regulation, Webcast, Webinar

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