Data Monitoring Committees

A Data Monitoring Committee (DMC) is an independent panel of experts who periodically meet during a study to review clinical data.  The primary purpose of a DMC is to protect the rights of current and future subjects in the trial by reviewing safety and exposure data and making recommendations to the study sponsor based on the results.  A DMC may recommend the study continue with no modification, with modification, or stop all together due to safety concerns.  The DMC may also be tasked with making recommendations based on interim efficacy results such as sample size modification or stopping criteria due to efficacy or futility.

Our DMC Experience

In addition to Data Monitoring Committees, we develop and organize many types of committees with various remits.   We are experienced in and can help you manage the following:

  • Data Safety Monitoring Boards (DSMB)
  • Independent Data Monitoring Committees (IDMC)
  • Safety Review Committees (SRC)
  • Data Review Committees (DRC)
  • Clinical Endpoint Committees (CEC) / Clinical Endpoint Adjudication

Veristat has managed over 45 DMCs in the last 5 years across numerous therapeutic indications including Cardiology, Endocrinology, Gastrointestinal Disorders, Genetic Disorders, Infectious Diseases, Neurology, Oncology and Pulmonology.

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Explore Our Data Monitoring Committee Services

  • Identify thought leaders in the relevant indication
  • Draft DMC Charter
  • Coordinate DMC meetings
  • Facilitate communication between study sponsor and committee members
  • Provide independent data analysis
  • Write meeting minutes
  • Generate safety reports
  • Manage safety and efficacy recommendations

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Contact Us Today

Utilize our team to plan and organize your clinical trial committee meeting to assist with data review, safety review or even clinical trial endpoint adjudication.    We can help recruit the committee members, draft the committe charter, run the meetings and more.

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