Patient Recruitment Using Our Unique FEP Method
When your clinical trial is delayed by slow subject enrollment, you need to quickly identify the issues impacting patient recruitment to find the best solutions. We are dedicated to provide you with excellence in patient recruitment strategies and services to improve outcomes – regardless of the clinical trial obstacles you face.
Documentation with Electronic Data Capture (EDC) expertise
We place a full-time, highly qualified clinical research coordinator at each study site to assist the investigators and site staffs with all day-to-day study conduct activities. Our coordinators are trained to provide professional support to the investigator ensuring compliance with FDA, local regulatory and ICH-GCP guidelines and efficient completion of assigned duties. The study coordinators are experienced in Electronic Data Capture (EDC) based trials. This helps in accurate data entry and thereby reducing queries from data management departments. Our Project Management and Quality Management Team carry out constant internal monitoring at the various sites to facilitate the documentation efficiently. This ensures collection of high quality study data necessary for regulatory and product approval submissions.
