We identify clinical research sites for sponsors and CROs efficiently with the highest quality service at the lowest possible cost. We help identify, contract, and supervise investigators and study coordinators. Additionally, We submit proposals to local ethics committees and health authorities, providing administrative and logistic support to investigational sites. All sites use central IRBs with short start-up regulatory document turnaround time, and are in full compliance with FDA, GCP, ICH, and IRB guidelines.
International Research Consultants
We get the Results you need !
