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The International Research Center conducts Phase I-IV clinical trials for the Biotechnology, Medical Device and Pharmaceutical industries. Our Clinical Trials conducted in our brand new state of the art Clinical Research Unit.The International Research Center conducts Phase I-IV clinical trials for the Biotechnology, Medical Device and Pharmaceutical industries. Our Clinical Trials conducted in our brand new state of the art Clinical Research Unit.
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The International Research Center conducts Phase I-IV clinical trials for the Biotechnology, Medical Device and Pharmaceutical industries. Our Clinical Trials conducted in our brand new state of the art Clinical Research Unit.
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Benefits

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

Clinical Trials

Clinical Expertise – The IRC professional staff provides years of experience and expertise in working with Phase I-IV sponsored trials.


Clinical Trials
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.


Clinical Trials
Rapid Remote Data Entry (RDE) – IRC provides timely, accurate research data entry for all clinical studies.


Clinical Trials
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.


Clinical Trials
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.


Clinical Trials
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.


Clinical Trials

Hands-on Principal Investigators (PI) – Our Principal Investigators are active with the clinical studies and present for the day-to-day operations.

 
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 - Texting with Trials   
 - IRC makes an imPACT   
 - IRC takes Vols to Lunch!   

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