Skip to content
  • Services
    • Medical Device Writing
    • Pharma/Biologics Writing
    • In Vitro Diagnostics Writing
    • Systematic Literature Reviews
  • Pricing
  • About CE
  • Resources
    • Blog
    • Webinars
    • FAQs
    • Careers
  • Services
    • Medical Device Writing
    • Pharma/Biologics Writing
    • In Vitro Diagnostics Writing
    • Systematic Literature Reviews
  • Pricing
  • About CE
  • Resources
    • Blog
    • Webinars
    • FAQs
    • Careers
Talk to an expert
4 events found.

Policy and Regulation

  1. Events
  2. Policy and Regulation

Events Search and Views Navigation

Event Views Navigation

  • List
  • Month
  • Day
Today
  • September 2021

  • Wed 1
    systematic literature review
    September 1, 2021 @ 11:00 AM - 11:45 AM PDT

    [Ask the Expert] Systematic Literature Review

    Virtual Q&A

    This session's topic: Systematic Literature Review: What is it and why is it so important? Do you have specific questions about the steps of the systematic literature review process or questions regarding your medical device or IVD? During this 45-minute Q&A session, our President Laurie Mitchell answers questions about the steps to conduct a methodologically […]

    Free
  • Wed 22
    safety and performance measures
    September 22, 2021 @ 10:00 AM - 10:45 AM PDT

    [Ask the Expert] Safety and Performance

    Virtual Q&A

    This session's topic: Safety and Performance Measures and Acceptance Criteria Do you have questions about how to identify meaningful safety and performance measures for the clinical evaluation? What are the best strategies for the verification of device safety and performance? During this 45-minute Q&A session, our President Laurie Mitchell answers questions on how to identify […]

    Free
  • November 2021

  • Wed 17
    November 17, 2021 @ 11:00 AM - 11:45 AM PST

    [Ask the Expert] Safety and Performance

    Virtual Q&A

    This session's topic: Safety and Performance Measures and Acceptance Criteria Do you have questions about how to identify meaningful safety and performance measures for the clinical evaluation? What are the best strategies for the verification of device safety and performance? Are you demonstrating that your safety and performance objectives are appropriate and clinically relevant​? Do […]

  • February 2022

  • Wed 9
    February 9, 2022 @ 11:00 AM - 11:45 AM PST

    [Ask the Expert] Safety and Performance (MDR)

    Virtual Q&A

    This session's topic: Safety and Performance Measures and Acceptance Criteria for MDR Do you have questions about how to identify meaningful safety and performance measures for the clinical evaluation? What are the best strategies for the verification of device safety and performance? Are you demonstrating that your safety and performance objectives are appropriate and clinically […]

  • Today
  • Next Events
  • Google Calendar
  • iCalendar
  • Outlook 365
  • Outlook Live
  • Export .ics file
  • Export Outlook .ics file

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

Twitter Youtube Linkedin

SERVICES

  • Medical Device Writing
  • Pharma/Biologics Writing
  • IVD Writing
  • Systematic Literature Reviews

RESOURCES

  • Webinars
  • Blog
  • FAQ's
  • Careers

ABOUT

  • About Us
  • Contact Us

© 2025 - CE LLC

This site uses cookies for functionality and analytics. Adjust your or review our privacy policy.

Privacy Overview

This website uses cookies so that we can provide you with the best user experience possible. Cookie information is stored in your browser and performs functions such as recognising you when you return to our website and helping our team to understand which sections of the website you find most interesting and useful.

Read more about our privacy policy here.

3rd Party Cookies

This website uses Google Tag Manager to collect information such as the number of visitors to the site, and the most popular pages. Keeping this cookie enabled helps us to improve our website.