Sponsor/CRO Info

Clinical Expertise & Experience

For over 30 years, our diverse team of medical professionals has provided consistent, high-quality research in a professional and ethical manner through collaboration with multi-national pharmaceutical, biotechnology and CRO companies on Phase I-IV clinical trials.

Cedar Crosse Research Center has conducted more than 550+ clinical trials across a wide range of therapeutic areas. Our board-certiﬁed investigators, experienced study coordinators and support staff are strictly compliant with Good Clinical Practice (GCP) and the changing dynamics of medical technology and clinical research. Using cost-effective management techniques, we yield superior quality data to progress studies faster for sponsor timelines and regulatory approval.

Dr. Danny Sugimoto founded Cedar Crosse Research Center in 1996 to make meaningful improvements in the lives of others through clinical research trials.

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Number of clinical trials completed with a multi-specialty therapeutic expertise including diabetes, hypertension, obesity, COPD, migraines, hyperlipidemia, etc.

Average cycle time in days from IRB submittal to IRB approval.

Principles of research

Care

A personalized, patient centered perspective in all clinical tasks.

Compliance

Strictly adhering to GCP and FDA regulatory procedures to quality date collections.

Compassion

Uniting with patients to improve lives.

100%

Randomization Rate

Experience

We have researched a wide variety of conditions with an expertise in General Medicine, Neurology & Psychiatry, Pulmonary, Pain Disorders, and more.

Site Support

We have an extensive support infrastructure to provide high quality data, rapid feasibility responses and streamlined communication.