Clinique Research Services, Inc. provides comprehensive site monitoring including the assurance of protocol compliance, accurate data capture, and GCP/ICH compliance at investigative sites.
Clinique Research Services, Inc. provides full project management support by assigning a Clinical Project Manger to communicate and manage all study activities.
- Help the investigator in screening patients
- Assisting investigators in the Informed Consent Process
Clinique Research Services, Inc. will personally train the investigator, study coordinator and study monitor on both US FDA 21 CFRs and clinical trial regulations to ensure collected data meets filing requirements in those countries.