Sponsors & CROs
Exalt Clinical Research occupies 2,000 square feet of dedicated research space and is connected to a large, secure parking garage. The site is equipped with 2 beds in private rooms for sleep studies, phase I and migraine trials. In-suite restroom, exam room, laboratory, administrative and clinical research coordinator space are ideal for efficient subject visits.
The site is located in the center of the revitalized, economically and ethnically diverse Chula Vista, less than 10 miles from the Mexico border and less than 15 miles from the San Diego International Airport. We are conveniently situated with easy public transportation access including bus, the San Diego Trolley, and taxi.
By simplifying the clinical trial experience, Exalt Clinical Research affords sponsors and CROs a single point of contact from subject identification and pre-screening to fully digitalized processes to clean data packaging. All of this is done through responsive communication practices throughout the life-span of the trial.
Our cohesive process of robust recruitment, best practices, and protocol execution provides sponsors and CROs the means to meet trial objectives in a timely and cost-effective manner.
Site Equipment and Diagnostic Services
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-4 Refrigerator
-20C Freezer
-80C Freezer
Calibrated Scale
Centrifuge
Centrifuge - Refrigerated
CLIA
CT
CTMS Database
DEXA Scan
Dry Ice
ECG
Electronic Source, Regulatory, Subject Data
Incubator
Mammogram
MRI
PET
Pharmacy
Phlebotomy - Fully equipped laboratory
Photography
Polysomnograms (PSGs)
Radiology
Sleep/Phase 1 Rooms
Therapeutic Indications
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Dermatology
Diabetes
Essential Tremor
Headache/Migraine
Healthy Volunteer
Obesity/Weight Loss
Sleep Disorders (in-Pt/out-Pt)
Smoking Cessation
Vaccine
Women’s Health
We are interested in hearing from you.
Your inquiry will go directly to Dixie L. Creager, Founder & CEO. A staff member will respond in 24 hours.
Or, you are welcome to contact our business development team at Ivy Clinical.
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Exalt means executing clinical research trials efficiently and effectively.
Mrs. Creager has orchestrated ground-up site development, innovative recruiting strategies, policy creation and integration, quality and compliance management, budget and contracting, and staff growth and development.
Further, when one of her sites was acquired by a larger entity, Mrs. Creager was invited to join a panel of internal scientific experts to assist the medical team in study assignment feasibility related to cost, staffing, and ability to perform accurately and timely on specific trials.
A wealth of experience gleaned in over 35 years in the clinical trials industry.