At Clinova CRO, we provide comprehensive clinical monitoring services to ensure the integrity and success of clinical trials. Our experienced monitors oversee every aspect of the study, ensuring compliance with Good Clinical Practice (GCP) and regulatory requirements. Our key clinical monitoring services include:

• Site Visits & Audits – Conducting regular visits to trial sites to ensure protocol adherence and data accuracy.
• Source Data Verification (SDV) – Ensuring that collected data is accurate and consistent with source documents.
• Risk-Based Monitoring (RBM) – Implementing strategic monitoring approaches to optimize trial efficiency.
• Regulatory Compliance Oversight – Ensuring adherence to FDA, EMA, and ICH-GCP guidelines.
• Investigator & Site Support – Providing guidance and training to investigators and site staff for smooth trial execution.