Access Clinical Research is a TURNKEY SOLUTION for your clinical trial patient recruitment. ACR coordinates all aspects of study trials, from ICH GCP training for the investigators and staff members, to contract negotiations and study management. Our service includes investigator recruitment, patient enrolment, identification and retention, IRB correspondence, database management, site management and regulatory compliance. ACR provides GCP and protocol training for PIs and CRCs, and a wide range of study-related management and operational activities covering all aspects of clinical trials. Our team of study-experienced professionals has the scientific capability and the management experience to conduct high-quality trials. With our patient database, our investigator network and clinical team have the medical expertise to work on specialty areas.