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  • June 2022

  • Wed 1

    Scoping Your MDR & IVDR Writing Projects

    June 1, 2022 @ 11:00 AM - 12:00 PM PDT
    Webinar , United States

    Scoping Your MDR and IVDR Writing Projects - The Forgotten Step In most of our webinars, we’ve focused on the writing process including which steps to take and how to organize your thoughts onto paper. However, we’ve never discussed what happens before the writing process begins. So what do you need before you get started? […]

    Free
  • Wed 15

    The Role of RA in the Clinical and Performance Evaluation Process

    June 15, 2022 @ 11:00 AM - 12:00 PM PDT
    Webinar , United States

    The Role of Regulatory Affairs in the Clinical and Performance Evaluation Process: Key Strategies to Support Project Success Regulatory Affairs plays a critical role in supporting the current MDR and IVDR required clinical/performance evaluation process, from project implementation through report writing and finally, the on-time submission to the notified body. From the early planning stage […]

    Free
  • July 2022

  • Wed 13

    ATE: The Role of RA in the Clinical and Performance Evaluation Process

    July 13, 2022 @ 11:00 AM - 11:45 AM PDT
    Virtual Q&A

    Ask the Expert: The Role of Regulatory Affairs in the Clinical and Performance Evaluation Process Regulatory Affairs is poised to play a critical role in supporting the current MDR and IVDR required clinical and performance evaluation process, from project implementation through report writing and finally, the on-time submission to the notified body. In this session, […]

    Free
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Criterion Edge

Criterion Edge is dedicated to advancing compliance and enhancing market success for Medical Device, Pharma, and IVD companies through industry leading writing services.

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