Observational Study Management
RCRSI is committed to the highest standards of professionalism and reliability while making our services widely affordable to the industry.
Support services for site preparation, patient enrolment, monitoring of data collection, and compliance to GCP to ensure smooth implementation of clinical trials. Shortening patient enrollment timelines, providing highest quality of data, minimizing staff turnover, ensuring transparency, timeliness and completeness of reporting of adverse events and data analysis and oversight of budget control.