What We Do


Clinical Event Committees

Our specialty is the management of CECs (clinical event committees). We have a long history of effectively managing all aspects of the CEC process from small, single centre trials to large multi-national, multi-centre trials. A list of some previous projects can be found here.

GCTP can perform and/or advise on:

  • CEC composition
  • CEC member identification
  • Endpoint data capture via eCRF
  • Endpoint process management
  • Scientific advice regarding selection of appropriate endpoints based on trial design
  • Endpoint definitions
  • Adjudication charter development
  • Integration of the CEC process within your trial framework
  • Investigative site and clinical study team training
  • Electronic Adjudication System development
  • Adjudication data packet assembly

GCTP works collaboratively with their clients to determine the approach that will best suit their unique needs. GCTP will handle the development of the endpoint process from start to finish, making delivery as simple and efficient as possible. GCTP services will be customized to our client’s specifications and requirements, ensuring the most cost-effective approach.



In addition to our Clinical Endpoint Committee services we can also provide advice on:

  • Trial design
  • Biostatistics
  • Protocol design
  • Regulatory strategy and submission planning

We would welcome engagement at any stage of your trial to help in its design and execution.

Want to work with us

We are always looking for new challenges and interesting partners.
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