Sana Research is committed to advancing medicine by helping sponsors develop new therapeutics to improve the lives our patients. We conduct high quality clinical trials that uphold the highest ethical and quality standards for our sponsors and patients.  We seek to enroll participants of all backgrounds and to increase the diversity of patients in clinical trials to reflect the composition of the general population. Fortunately being located in the Northern Virginia area, our community is very ethnically and culturally diverse. 

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Our clinical research team has robust experience conducting trials that provide accurate and high quality data. Our team includes 4 investigators who are board certified in neurology and 1 investigator board certified in cardiovascular diseases. Collectively, we have been involved more than 40 studies in the following therapeutic areas:

• Alzheimer's Dementia

• Stroke

• Epilepsy

• Cardiovascular Disease

  • Acute Coronary Syndromes

  • Heart Failure

  • Lipoprotein (a)

• Obesity

• Platelet Thrombosis

• Biomarkers (hstroponin, nt-proBNP)​

Our full time staff of investigators, coordinators, regulatory staff,  and other support groups are committed to working closely with sponsors and CROs throughout the entire process, including: feasibility, site evaluation, investigator selection, study initiation, enrollment, monitoring visits, quality assurance, data entry, and study closeout.

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We can initiate studies quickly by using a central IRB. To help fulfill the FDA mandate to increase diversity in clinical trials, Sana Research can conduct studies in Spanish and Vietnamese as well with our bilingual staff.

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Once on site, monitors and sponsors have access to:

• Convenient underground parking

• Private secured high speed WIFI

• Copier

• Fax Machine

• On-site cafeteria

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