Clinical trial monitoring
Clinical trial monitoring is a crucial aspect of ensuring the integrity, safety, and compliance of a clinical study. It involves the ongoing oversight of clinical trials to confirm that they are conducted in accordance with the study protocol, regulatory requirements, and Good Clinical Practice (GCP) guidelines. Monitoring ensures that data collected is accurate, complete, and verifiable, while also safeguarding the well-being of participants.
Our skilled Clinical Research Associates (CRAs) are therapeutically specialized and receive centralized training. To maintain consistent execution, we offer extensive, continuous in-house training programs for all team members. Our CRAs possess RN, BS, or MS degrees in scientific fields, are multilingual, and are based across the globe. Through our global affiliates, Neuvantics can also meet monitoring requirements worldwide. Our wide geographic presence enables us to deliver high-quality, cost-effective monitoring for clinical trials, regardless of site or patient location.
Our Clinical trial monitoring services include:
- Recruitment and Retention Support
- Investigator and Site Performance Evaluation
- Monitoring of Protocol Deviations
- Investigational Product Accountability
- Audit and Inspection Support
- Monitoring of Study Timelines and Milestones
- Safety Data Review and Management
- Remote Monitoring Services