ICRC is the ideal for Sponsors and CRO's
We deliver consistent, compliant, high-quality results with a patient-centered research management model.
Trial Participants
ICRC uses a thorough study feasibility process involving pre-identifying prospective participants through Electronic Medical Records. This ensures that your study is populated with qualified and motivated individuals. Our recruitment team works tirelessly to implement fully integrated programs that consistently yield high patient recruitment rates, retention, and satisfaction. Our success rates in these areas continue to exceed the industry average.
Professional Team
The ICRC has partnered with specialized physicians and healthcare institutions to conduct clinical trials. Our network integration systems and geographic proximity facilitate the sharing of research staff and collaboration among physicians, ensuring every project's success. Our quality assurance and regulatory department ensures that all team members are trained and compliant. Meanwhile, our internal project management services simplify the contracting process for this multi-site network, providing a single point of accountability.
Clinical trials are a viable care option for individuals seeking treatment.
Integrated Clinical Research Center is an organization dedicated to clinical research results. Our site management services offer unique solutions including Faster recruitment, increased patient enrollment per site, enhanced data quality and timeliness, reduced data queries, improved GCP compliance, utilization of eSource, and remote monitoring.