Overview

We are a unique research company with over 28 years of experience conducting clinical trials for the pharmaceutical industry. We specialize in Phase II, III, and Phase IV clinical trials.

Mission Statement: To provide the highest quality service to our sponsors and host clinics, while maintaining patient safety. To support a work environment which promotes teamwork and personal growth for our employees.

Experience

Our sites have completed more than 800 clinical trials. The sites consist of Family Practice physicians along with sub-specialists in Allergies, ENT, Emergency Medicine, Internal Medicine, Neurology, OB/GYN, and Pediatrics.

We have conducted studies in the following areas: Asthma, Allergic Rhinitis, Contraception, Dermatology, Depression, Diabetes, Heartburn, GERD, IBS, Hypertension, Hyperlipidemia, Impotence, Infectious Diseases: CAP, AECB, Sinusitis with/without puncture, Skin Infections, Otitis media and externa, Cold, Influenza, and UTI, Migraine, Musculoskeletal (sprains and contusions), Osteoarthritis, OTC indications, Pain, Pediatrics, Urology, Vaccines, and Women's studies.

Facility

We are located at five clinics in the Salt Lake City area. Four of our clinics are family practice clinics and one is an urgent care facility. We conduct outpatient studies. Two of our clinics are open 7 days a week and the other three clinics have the availability of seeing subjects 7 days a week. We are on call 7 days a week, 24 hours per day. We have on site labs, x-ray, bone densitometry, EKG, ultrasound, -20 degree freezer, -70 degree freezer, and a refrigerated centrifuge.

We have easy access to the Salt Lake International Airport and accommodations near each of our clinics.

Investigator

We work with seven different principal investigators with research experience from 10 to 26 years. Our principal investigators are trained on GCP's, ICH guidelines, and the FDA Code of Regulations. Because we are consistently top enrollers on most of the studies we conduct, we have many years of experience in audits.

Staff

We have a fully dedicated full-time RN clinical research coordinator staff, as well as trained CRC’s. We are experienced in both Sponsor and FDA audits. We are committed to working as a team with the Sponsor, CRO, IRB, and patients to deliver safe quality patient care and excellent data.

Patients

Because of our close long term physician-patient relationship, we enroll the majority of our patients from our clinics. We have a large data bank of patients from which to draw. We know our patients so we have a high retention rate. Our goal is always to meet or exceed enrollment targets in a timely fashion without jeopardizing quality.

Other

• Our sites use a central IRB
• Our goal is to complete and return regulatory packages within 48 hours
• Contracts are generally reviewed and returned within 1 week
• We work with 37 investigators and sub-investigators

Our staff includes:

• 5 managers
• 20 full-time Clinical Research Coordinators
• 6 Clinical Research Assistants
• 2 Accountants
• 1 Clinical Regulatory Specialist

Normal study load is 3 studies for each CRC