[FREE WEBINAR] Eliminating the Guesswork: What you need to know about Endpoint Adjudication by the CEC

By: Sarah VanVickle Chaves, Director of IVD and Scientific Writing Services, Ph.D. Molecular and Cellular Biology

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.

TALK TO AN EXPERT

Whether you’re navigating a complex regulatory submission, preparing for an audit, or simply exploring outsourced support — our team is here to help.

Criterion Edge specializes in high-quality, compliant medical writing services for the life sciences industry. Use the form to tell us a bit about your needs — one of our experts will follow up within one business day.

Need a faster response? Use the chat icon in the lower-right corner to speak with us immediately during business hours.

  • No obligation — just an open conversation
  • Expert guidance from PhD-level writers
  • Trusted by leading MedTech & Pharma companies
  • Fast turnaround for time-sensitive projects
  • Clear quotes and scoping available

How Can We Help?

TALK TO AN EXPERT

Whether you’re navigating a complex regulatory submission, preparing for an audit, or simply exploring outsourced support — our team is here to help.

Criterion Edge specializes in high-quality, compliant medical writing services for the life sciences industry. Use the form to tell us a bit about your needs — one of our experts will follow up within one business day.

Need a faster response? Use the chat icon in the lower-right corner to speak with us immediately during business hours.

  • No obligation — just an open conversation
  • Expert guidance from PhD-level writers
  • Trusted by leading MedTech & Pharma companies
  • Fast turnaround for time-sensitive projects
  • Clear quotes and scoping available

How Can We Help?

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