Data Review Committees in Clinical Trials

Ensuring patient safety through an independant non-biased panel is critical in every clinical program.   

A Data Review Committee (DRC) is an independent panel of experts who periodically meet during a study to review clinical data.  The primary purpose of  is to protect the current and future patients in the trial by reviewing safety and exposure data and making unbiased recommendations to the study sponsor based on the results.  A DRC may recommend the study continue with no modification, with modification, or stop all together due to safety concerns.  The DRC can also make recommendations based on interim efficacy results - particularly in adaptive design trials -  sample size modification or stopping criteria due to efficacy or futility.

Data Review Committee Expertise

Veristat teams develop and organize many types of data review committees with various remits.   We are experienced in and can help you manage the following:

  • Data Monitoring Committees
  • 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 DRCs in the last 5 years across numerous therapeutic indications including Cardiology, Endocrinology, Gastrointestinal Disorders, Genetic Disorders, Infectious Diseases, Neurology, Oncology and Pulmonology.

ebola-data-monitoring-committee

Contact Veristat Now


Request A Proposal

Contact Us


 Data Review Committee Services

people_working_woman_image3_opt1200px
  • 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

people_working_image2_opt1200px
Explore-More-Image-1

Explore more of our impactful Service Offerings.

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.

Contact Us

Contact Us
Request A Proposal