We connect pharmaceutical and
device companies with patients and
physicians to help provide cutting-
edge therapies for a variety of
At Injury Care Research and Family Care Research, we recognize that competent and ethical clinical research coordinators are the core of successful clinical trials. We ensure all staff undergo and maintain comprehensive training in GCP/ICH, IATA and HIPPA regulations. All coordinators have extensive experience with numerous eCRF and eDiary systems. To ensure quality we also have a comprehensive internal audit and QA program.
We also understand that quick study start-up and rapid recruitment is key to successful trials. We have a 72-hour turnaround time for regulatory documents, and clinical trial agreements are typically executed within seven days. We do not need a finalized CTA in place to complete regulatory documents. Strategically competitive and consistently high enrollers, we are known to be effective in our approach to clinical trials. Our recruitment efforts are successful by conducting thorough database reviews and utilizing TV, radio, print, and online media. We are also known for our strong community ties through health fairs and alliances with various local foundations and clinician referrals.
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