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We have always believed that patients of private practitioners provide better research data - real patients in real medical settings, interacting with their own medical doctor, resulting in better overall data reliability.

We have always known that the success of clinical trials revolves around the coordinators and study staff team. We integrate our knowledgeable coordinators into the offices of our longstanding partners in private practice. These study-dedicated individuals relieve office nurses and staff of the often overwhelming additional responsibilities that come with good, compliant research.

Tidewater Clinical Research is a partnership between physician investigators and trials management teams. Each having ownership in the outcome.

Our reputation is one of efficiency and effectiveness. We boast exceeding enrollment goals in over 98% of our trials.  Our successful partnerships have resulted in repeat trial opportunities from very satisfied Sponsors and CROs.

We have dedicated teams for every project lead by ACRP certified coordinators and coordinator-managers with over eighteen years research experience. We can use Central IRBs. Regulatory documents, contracts  and budgets can be turned around within two business days. We have vast experience with electronic data capture and electronic patient diaries, as well as paper forms - CRFs are always completed within 24 hours of a subject visit.




 
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