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Abstract
A privately held, 17-year-old company located in Strongsville, Ohio, IMARC assists the clinical research community in the pursuit of FDA and worldwide approvals. IMARC is a medical device CRO whose effectiveness is built on our commitment to human subject protection and our dedication to ensuring study compliance in our partnership with clients. IMARC's approach -- based solidly in both U.S. and international regulations -- results in the support, proof and assurance researchers seek to overcome chaos caused by complexity, while achieving compliance through consistency. Providing committed, competent and confident consultation is how IMARC sets the highest standards for site outcomes and study partnerships.