AN OVERVIEW OF OUR SERVICES

STUDY ADMINISTRATION

One contract and one point of contact. This allows site identification, feasibility and study start up to occur at an accelerated pace.

GCP TRAINED PI AND SITE PERSONNEL

Our site has dedicated research staff consisting of highly trained, board certified investigators, study coordinators, patient recruiters and support staff.

FAST AND EASY FEASIBILITY DETERMINATION

Start up time is critical to the success of a clinical trial as delays translate directly into lost revenue. Sponsors benefit from our experience and efficient management. Our staff's ability to quickly complete feasibility questionnaires  allows a clinical trial to begin without delay. Facilitation of rapid site activation saves time and reduces costs.

AGGRESSIVE RECRUITMENT AND RETENTION

With the continuous recruitment throughout our studies, we are able to rapidly enroll a study with the required demographics. Our company sets itself apart with a proven record of success to start a study successfully; sponsor trials are conducted on time and fully enrolled with the right subjects for the right study.

We are compliant with SOPs, HIPPA and research specific requirements. Our resources and equipment meet the requirements of today’s demanding studies.

Our company  is in full compliance with FDA, GCP, ICH and IRB guidelines. Our highly trained and efficient staff delivers exceptional levels of service completed with the utmost professionalism and provide sponsors with reliable, quality data.