Tech-Clarity

Making the value of technology clear

  • Published Research
    • eBooks
    • White Papers
    • Survey Results
    • Buyer’s Guides
    • Infographics
  • Research Invitations
    • Survey Invitations
    • Assessments
  • Presentations & Videos
    • Webinars
    • Live Presentations
    • Tech-Clarity TV
    • Virtual Events
  • Insights & Activity
    • In the News
    • Insights
  • About
    • Team Tech-Clarity
    • Jim Brown
    • Michelle Boucher
    • Julie Fraser
    • Rick Franzosa
    • Arvind Krishnan
  • Search
  • Search
  • Date

FDA

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,…

Read More →

  • Tech-Clarity TV

Jim Brown - February 20, 2018 - Filed Under: Presentations & Videos, Tech-Clarity TV, Video - Tagged With: Digital Enterprise, DMR, 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

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…

Read More →

  • Buyer's Guides

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

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….

Read More →

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

    Medical Device Engineering

    Selecting the Right PLM Software for Medical Device Engineering (webcast)

    Listen to Tech-Clarity’s Michelle Boucher, Mark Turner from Alcon Labs (Novartis), and Swapan Jha from PTC have a discussion on the right software solution for medical device engineering. The discussion featured an interactive discussion between the panelists coving topics such as: Challenges facing medical device manufacturers. Why to consider the complete product lifecycle with respect…

    Read More →

    • Webinars

    Michelle Boucher - September 11, 2017 - Filed Under: Presentations & Videos, Webinars - Tagged With: Regulation, Traceability, Cost of Compliance, IoT, Compliance, Engineer, PLM, FDA, PTC, Smart Connected Products, ALM, Medical Device, Webcast, Webinar

    Cost Effective Quality in CPG (webcast, survey results)

    Join Tech-Clarity’s Jim Brown on this webinar sharing  recent survey results from almost 200 Consumer Packaged Goods companies, delving into their quality issue and how top performing CPG companies achieve better quality without suffering from excess internal cost. Learn the process, organizational, and technology approaches that Top Performers leverage to overcome their challenges and drive cost-effective quality. This Business…

    Read More →

    • Webinars

    Jim Brown - June 7, 2017 - Filed Under: Presentations & Videos, Webinars - Tagged With: Cost, Best Practices, Webcast, Webinar, CPG, Consumer Packaged Goods, Food and Beverage, Survey, Audit, QMS, FDA, Quality, Cost Effective, Quality Management

    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…

    Read More →

    • Webinars

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

    • « Previous Page
    • 1
    • 2
    • 3
    • Next Page »
    Join our community to receive our newsletter and survey invitations.

    Copyright © 2012-2024 – Tech-Clarity, Inc.

    • Contact
    • Privacy Policy
    • Date

    • LinkedIn
    • Facebook
    • LinkedIn
    • Facebook

    Copyright © 2012-2024 – Tech-Clarity, Inc.