The Rebecca D. Considine Research Institute at Akron Children’s Hospital provides a centralized approach to meeting the needs of clinical study sponsors. As a clinical study site since 2000, we have met diverse needs of the medical research community, including those of the NIH, foundations, pharmaceutical companies, contract research organizations, and investigator-sponsored trials.
Our range of expertise encompasses all major drug development and approval study models, from Phase 1 to Phase 4 trials as well as post-marketing surveillance studies. We have in-depth experience complying with federal and state regulations for human subject research protection.
Our full-time staff serves inpatient and outpatient populations and includes regulatory experts, study coordinators, research nurses, bioinformatic and biostatistical support. We are committed to coordinating every aspect of research site support.
We offer study sponsors seamlessly integrated clinical research management capabilities:
If you would like to discuss your clinical study research needs, contact Eloise Lemon, RN, BSN,CCRC, administrative director of clinical services, at 330-543-3193 or firstname.lastname@example.org.
You may also fax information to 330-543-3166.
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