Adequate Monitoring of Clinical Trials is imperative in assuring safe subjects, quality data and a well-executed study.  Clinique Research Services, Inc. provides comprehensive site monitoring including the assurance of protocol compliance, accurate data capture, and GCP/ICH compliance at investigative sites. Our CRA’s act as a liaison between the site and the study teams.  Monitoring visits are conducted at pre-determined intervals and/or as the study dictates.