Norwich Clinical Research Associates Ltd. (NCRA) provides clinical research services to the pharmaceutical, medical device, nutraceutical and related industries. Our primary product is the completion of clinical research projects on time and on budget. We accomplish this with a stable group of highly skilled and experienced teams of professional and technical staff who have substantial multi-disciplinary industry experience and accomplishments. Our expertise with fax-based data acquisition and in specific project management, results in substantially increased speed and efficiency for completion of each clinical research project that we undertake.
NCRA is a full service contract research organization but we also like to think of ourselves as a Critical Resource Organization. We will bring you what you need in qualified, supplemental resources and services quickly when you require them—our teams are ready and will help you achieve your goals.

Our Associates have many years of experience in the industry, regulatory, clinical and academic arenas, which enables us to see clinical development from all sides of the process.  We contract to conduct either parts of or whole projects for compound/drug, device or nutraceutical development according to client needs.

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:

  • in-life segments (computerized trial management and management reports),

  • data management (remote [DataFaxÔ] and conventional data entry, data-base preparation),

  • clinical trial monitoring with Medical Monitors and experienced Clinical Research Associates,

  • statistical analysis, and

  • final report and other technical and medical writing services.