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ALM

MedTech ALM and PLM

MedTech: ALM and PLM Better Together

What should MedTech companies consider when integrating ALM and PLM? Software has become a crucial component in MedTech products. However, with software development managed in Application Lifecycle Management (ALM) and hardware managed in Product Lifecycle Management (PLM), the separate systems can create silos within the product development team. With increasing regulatory pressures and trends such…

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  • Webinars

Michelle Boucher - May 20, 2025 - Filed Under: Webinars, Presentations & Videos - Tagged With: Compliance, PLM, ALM, Digital Thread Integration, Medical Device, MedTech, Embedded Software, Digital Thread, Med Device

ALM and PLM

Integrating ALM and PLM Buyer’s Guide

How do you accelerate the co-development of hardware and software for your products? Today’s products increasingly rely on software for innovation. Yet, development teams follow different processes and use separate tools to support the engineering and development of hardware and software. This creates silos within the development team that causes breakdowns in communication and hurts…

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  • Buyer's Guides

Michelle Boucher - March 11, 2025 - Filed Under: Buyer's Guides, eBooks, Published Research - Tagged With: SoftwareDevelopment, ProductDevelopment, PLM, Engineering, Innovation, HardwareDevelopment, ALM

Aras ACE

Aras Showcases Differentiation and Strengths at ACE 2023 (Insight)

ACE is Back! PLM conferences are back, and it seems there’s a conference a week right now! The first one I attended this Spring was Aras’ ACE conference. This was a special one for me because it was my first time attending in person. I was planning to attend in 2020 but it was canceled…

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  • Insights

Jim Brown - June 8, 2023 - Filed Under: Insights, Insights & Activity, Slideshow - Tagged With: PLM, Aras Corporation, Ansys, ALM, Aveva, Aras, SPDM, Cloud, Conference, Aras Innovator, Review, Low-Code

Medical Device Manufacturers’ Software

Medical Device Manufacturers’ Software Selection 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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  • White Papers

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

EU MDR

EU MDR: How Abbott is Getting Their Digital House In Order (webcast)

If you are in the medical device industry, are you prepared for the EU MDR? In this on-demand webcast, Tech-Clarity’s Michelle Boucher interviews Caroline Byrd, regulatory expert at Abbott, about the steps Abbott has taken to prepare product data for EU MDR compliance. They discuss: Significant changes between the MDD and MDR How to prioritize…

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  • Webinars

Michelle Boucher - November 1, 2018 - Filed Under: Webinars, Presentations & Videos - Tagged With: Medical Device Regulation, Webcast, EUDAMED, Webinar, Regulation, Traceability, Cost of Compliance, Engineer, Compliance, Single Source of Truth, PLM, Abbott, PTC, EU MDR, ALM, MDD, Medical Device

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: Quality Management, FDA, CAPA, Case for Quality, Regulations, ISO 13485, Medical Device, UDI, Requirements, Embedded Software, Compliance, Healthcare, PLM, Criteria, Product Development, Buyer's Guide, ALM, IoT, NPD, Internet of Things

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