At Clinova CRO, we provide comprehensive site management solutions to ensure smooth and successful clinical trials. Our experienced team works closely with investigators, sponsors, and research teams to streamline operations and maintain regulatory compliance. Our key site management services include:

• Site Selection & Activation – Identifying and preparing high-quality research sites for clinical trials.
• Investigator Support & Training – Providing guidance and resources to ensure protocol adherence.
• Regulatory & Ethics Compliance – Managing documentation and approvals for seamless trial execution.
• Patient Recruitment & Retention – Implementing strategies to enroll and retain eligible participants.
• Site Performance Monitoring – Conducting regular assessments to optimize trial efficiency.