2. Overall Execution of Study On-Site
We provide comprehensive on-site study management and execution services, ensuring that clinical trials are conducted efficiently and in full compliance with the protocol and regulatory requirements. Our on-site support includes patient recruitment strategies, informed consent process, meticulous data collection, source document verification, and site-level quality control, optimizing trial performance and data integrity directly at the research site.
Key Aspects of This Service:
- Site Management: Efficient day-to-day management of study activities.
- Patient Management: Effective recruitment and retention strategies.
- Data Collection: Accurate and timely data acquisition.
- Protocol Adherence: Ensuring strict compliance with study protocols.