Ensuring Study Integrity Throughout Your Programs
With rich experience in clinical trials and a high-quality, professional Clinical Research Associate (CRA) team, MAVEN provides comprehensive monitoring of all project functions and parameters to ensure the integrity of your program.
Our extensive range of services covers phase I–IV clinical trials of drugs and device development in all major therapeutic areas. Our robust training system ensures every CRA has clinical research experience, regulatory knowledge, and work skills to provide quality services that are consistently trusted and recognized by our partners.
Get Expert CRAs to Rigorously Monitor Clinical Activities at Every Stage
- Site selection visit
- Site initiation visit
- Interim monitoring visits
- Closeout visit
