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Norwich Clinical Research Associates |
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 Norwich Clinical Research Associates Ltd. (NCRA) has been providing quality clinical research services since 1994. Our primary product is the completion of clinical research projects accurately and cost effectively. NCRA offers competitively priced clinical research services to the pharmaceutical, medical device and nutraceutical industries. If you are seeking a Contract Research Organization (CRO) highly capable of forwarding your product development objectives, yet flexible enough to meet your changing needs, we believe we are the CRO you need.
NCRA specializes in pre- and post-marketing studies and are especially skilled in clinical monitoring, auditing, and data management services uniquely needed for the pharmaceutical, nutraceutical, medical device and biotech industries. Additional services NCRA provides are statistical analysis, processing and writing final reports and regulatory documents, assistance with developing standard operating procedures, plus training on conduct and monitoring of regulated clinical trials. NCRA conducts clinical trials in entirety from protocol design to completion of the final reports for regulatory submission. The Company's associates are experienced in preparation and completion of FDA regulatory applications
NCRA is a full service contract research organization but we also think of ourselves as a Critical Resource Organization. We can bring you the qualified, supplemental resources and services that you need quickly when you require them—our teams are ready and will help you achieve your goals. We provide valuable strategic and tactical advice, as well as product development and marketing strategy consultations that enhance the probability for your success in meeting your product development goals. NCRA’s individual disciplinary teams conduct and complete any or all segments of clinical trials:
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