Resources for MDR & IVDR

Medical device scan

Automation for MDR & IVDR: A Three-Part Seminar

Describes key content automation technologies and how they address the requirements of MDR & IVDR translation compliance.

  • Webinar

    Part 1: What is a CCMS and How Does It Address the Challenges Posed by MDR & IVDR?

  • Webinar

    Part 2: Structured Content and CCMS Technology to meet MDR & IVDR requirements: Takeda Medical Device Group, Qserve, & TransPerfect Medical Device Solutions

  • Webinar

    Part 3: EnCompass Step by Step: A Detailed View of the Content Automation Solution to Meet MDR & IVDR Requirements

More MDR & IVDR Automation Information

Discover additional strategies for leveraging automation in your MDR/IVDR initiatives

  • Webinar

    Future-Proof Content: Key for Success

  • Webinar

    AI for MDR & IVDR Success

  • Webinar

    Medtronic Uses AI for PMS

  • Webinar

    Automation for MDR & IVDR PMS Requirements

  • Webinar

    Marketing Content Under MDR & IVDR

  • Webinar

    Don’t Wait, Automate! Intelligent Automation for MDR/IVDR Success

Translation and Localization for Websites, Apps, Software, E-Learning, and Other Digital Content

  • Webinar

    Translation & Localization for Software & IVD Devices

  • Webinar

    Translation & Localization for E-Learning & Training

MDR and IVDR Timeline Overview

In order to take advantage of the MDD extension, device manufacturers must comply with several near-term deadlines and plan for long regulatory turnarounds – the extension provides less time than you might think! Learn how TransPerfect can help you meet the impending MDR and IVDR deadlines with intelligent automation solutions for labeling, SSCPs, SSPs, marketing and other regulated content by downloading our MDR/IVDR deadlines cheat sheet!

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MDR and IVDR Timeline Overview

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