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Healthcare

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

CAD

Healthcare Survey: Help make in silico clinical trials a reality (survey invite)

Would greater regulatory support for in silico clinical trials help you? What are best practices to support personalized healthcare? How are other companies using in silico clinical trials and what benefits do they see? We are conducting new research on the healthcare industry to explore these questions and more. If you work in the healthcare industry,…

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Michelle Boucher - August 7, 2018 - Filed Under: Uncategorized - Tagged With: clinical trials, Digital Twin, Engineer, Healthcare, in silico, Innovation, MBD, Medical Device, personalized healthcare, Pharmaceutical, Simulation, Survey, Survey Monkey

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 Manufacturers Software Selection Guide

Tech-Clarity’s Medical Devices Manufacturers Software Selection Guide helps manufacturers identify the right buying criteria for software solutions to support developing, producing, and servicing medical devices. This buyer’s guide also takes into account unique needs for medical device companies including regulatory compliance and support for the FDA’s Case for Quality. Tech-Clarity’s Buyer’s Guides go beyond software functionality to…

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Michelle Boucher - February 23, 2017 - Filed Under: Published Research - Tagged With: ALM, Buyer's Guide, Case for Quality, Compliance, Criteria, Embedded Software, FDA, Healthcare, Internet of Things, IoT, Medical Device, NPD, PLM, Product Development, Quality Management, Regulations, Requirements

Securing Market Access for Medical Devices

Jim Brown will join Supply & Demand Chain Executive and IHS to help healthcare companies understand how the market for their products can be put at risk by regulations and supply chain issues such as counterfeit components and shortages. View a Replay of the Webcast

Jim Brown - April 6, 2012 - Filed Under: Presentations & Video - Tagged With: Compliance, Counterfeit, Healthcare, Medical Devices, Supply Chain, Webcast

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