Join Criterion Edge’s VP of Scientific and Medical Affairs, Kyoko Hattori for an informational webinar on Endpoint Adjudication by the Clinical Endpoints Committee.
Date/Time: September 12th, 2018 at 11 AM PST/2 PM EST
Kyoko brings over 30 years of expertise to share with clinical field scientists and managers, drug safety specialists, medical monitors, and more. Join Kyoko and other senior professionals during the webinar to learn more about familiarization and guidance using endpoint adjudication by the CEC.
Kyoko will be discussing CEC regulatory guidance as well as influencing factors in using a CEC in clinical trials. Be a part of the discussion as she describes common sources and tools needed for adjudication, as well as methods used to identify adjudicable events using site-reported data. Kyoko will address event processing practices and pitfalls and cover several common questions concerning adjudication.
The 30 minute presentation will be followed by a 30 minute Q&A for further attendee discussion and participation. The webinar will be sponsored by Emanate Life Sciences and Criterion Edge.
Unable to tune in on September 12th? Click here to view the recording.
If you missed our last webinar on Adverse Event Reviews, you can find it here.
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We had a large turnout at our webinar on April 29, 2020, “How to Assess Your CER for MDR Readiness, Part 1 : State of the Art, Safety & Performance Criteria, Equivalence and Systematic Literature Review.” We ended with many unanswered questions. To answer these and more questions, President Laurie Mitchell is coming back to host a Question & Answer session LIVE.
Jun 4, 2020 11:00 AM in Pacific Time (US and Canada)