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How Technology is Transforming Clinical Endpoint Adjudication

Thursday, June 17, 2021 (11:00 AM - 12:00 PM) (EDT)

Description

When clinical endpoints are subjective, image-based or complex to assess or the study is geographically broad, researchers of new drugs and devices may find it difficult to demonstrate acceptable safety results to regulatory authorities. 

To meet this requirement, trial sponsors and Contract Research Organizations (CROs) are turning to Clinical Endpoint Committees (CEC) for independent event adjudication as the most efficient process to help reduce costs, increase quality, and eliminate clinical bias. Traditional manual, paper-based approaches to CEC management place significant time, cost, and resource burdens on organizations - and are prone to errors, bias and regulatory issues. 

As with many other areas of clinical research, innovative new technologies – when combined with scientific and medical expertise – are helping to remove these barriers and drive significant gains in efficiency, accuracy, data quality, and compliance. Today’s web-based adjudication systems offer advantages that inefficient paper-based processes cannot. 

Learn from the experts about: 

  • How technology can transform clinical endpoint adjudication 
  • The keys to successful implementation 
  • The must-haves when selecting the right solution 
  • How it fits into the regulatory landscape 

Learn more

Event Contact
Brian Johnson
Thursday, June 17, 2021 (11:00 AM - 12:00 PM) (EDT)
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