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.
- Site selection/investigator qualification
- Site initiation
- Routine monitoring
- Risk-based monitoring
- Centralized monitoring
- Study close-out
- TMF management
MedTrials offers extensive clinical trial managemet expertise. We employ highly-trained clinical research professionals and deploy time-tested procedures to ensure you receive the right solutions for each study from start-up to close-out.Learn More
Highly trained and qualified clinical research associates (CRAs) ensure your sites research activities are conducted, recorded, and reported in accordance with the study protocol and the applicable regulatory requirements.Learn More
Timely payment of investigators and study subjects directly correlates to clinical trial performance. MedTrials provides an end-to-end solution for clinical grants administration from budget negotiation and contracting to site compensation and associated tax and regulatory reporting.Learn More