MedTrials' Monitors Ensure Collaboration Between Sponsor And Their Investigative Sites

MedTrials highly trained and qualified clinical research associates (CRAs) oversee the progress of a clinical trial to ensure that it is conducted, recorded, and reported in accordance with the protocol, Standard Operating Procedures (SOPs), Good Clinical Practice (GCP), and the applicable regulatory requirements.

Monitoring activities ensure that clinical trials are conducted and documented properly. Our monitoring teams, including field and in-house CRAs, work closely together on project execution, training, and problem solving. We promote a monitoring and site management approach that utilizes open communication and collaboration with the sponsor and the investigative sites.

Services include:
  • Site selection/investigator qualification
  • Site initiation
  • Routine monitoring
  • Risk-based monitoring
  • Centralized monitoring
  • Study close-out
  • TMF management

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