Resources for MDR & IVDR
Automation for MDR & IVDR: A Three-Part Seminar
Describes key content automation technologies and how they address the requirements of MDR & IVDR translation compliance.
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WebinarPart 1: What is a CCMS and How Does It Address the Challenges Posed by MDR & IVDR?
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WebinarPart 2: Structured Content and CCMS Technology to meet MDR & IVDR requirements: Takeda Medical Device Group, Qserve, & TransPerfect Medical Device Solutions
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WebinarPart 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
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WebinarFuture-Proof Content: Key for Success
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WebinarAI for MDR & IVDR Success
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WebinarMedtronic Uses AI for PMS
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WebinarAutomation for MDR & IVDR PMS Requirements
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WebinarMarketing Content Under MDR & IVDR
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WebinarDon’t Wait, Automate! Intelligent Automation for MDR/IVDR Success
Translation and Localization for Websites, Apps, Software, E-Learning, and Other Digital Content
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WebinarTranslation & Localization for Software & IVD Devices
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WebinarTranslation & Localization for E-Learning & Training
Medical Device Regulation: Less Time Than You Think?
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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