Benefits
Sponsoring a clinical trial study at IRC reaps a number of benefits for your organization. |

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Clinical Expertise – The IRC professional staff provides years of experience and expertise in working with Phase I-IV sponsored trials.
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Regulatory Affairs – Our experienced regulatory staff provides prompt, accurate document submissions for clinical trials. The turnaround time for receipt to submission of new regulatory documents is within five (5) business days, which accelerates the start-up process. In addition, the staff provides a centralized regulatory body for the duration of the study.
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Rapid Remote Data Entry (RDE) – IRC provides timely, accurate research data entry for all clinical studies.
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Quality Assurance – IRC has an external Quality Assurance person who conducts independent audits to verify study and site conformity with IRC's standard operating procedures and regulatory requirements.
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Recruitment Center – Our unique recruitment strategy provides a customized and dynamic plan for each of your studies. Our active database enables us to quickly identify a vast number of potential volunteers for a variety of clinical studies.
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Patient Retention – IRC regularly follows up with volunteers to ensure their overall well-being and study participation. For all volunteers, we offer a “pick-up” and “drop-off” service in an effort to provide travel safety and timely study attendance.
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Hands-on Principal Investigators (PI) – Our Principal Investigators are active with the clinical studies and present for the day-to-day operations. |