SERVICES

Our work is to conduct clinical trials for the pharmaceutical industry.  We focus on phases I through IV on interventional, observational and device medical research.​

AREAS OF THERAPEUTIC INTEREST

  • Alzheimer’s Disease

  • Anemia

  • Asthma

  • Chronic Kidney Disease

  • Contraception

  • Depression

  • Dermatitis

  • Diabetes

  • Esophagitis

  • GERD/NERD

  • High Blood Pressure (Hypertension)

  • Hyperlipidemia

  • Hypo/Hyperthyroidism

  • Menopause

  • Migraine

  • Obesity

  • Osteoarthritis

  • Psoriasis

  • Smoke Cessation

Participants are closely followed by a devoted and knowledgeable staff lead by our board-certified physicians and do not have to pay anything for the medical care, investigational medications and diagnostic tests they receive.  In case any doubt arises, follow the FAQ link or let us know, we will reply as soon as possible.

Image by Matt C

FACILITY

  • Within 5 minutes of major hospital

  • On site CLIA-waived laboratory processing and IATA packaging station

  • Yearly calibrated equipment, -20 and -70 freezers and backup generator

  • Locked and daily monitored medication storage (refrigerated and ambient)

  • Secure off site records storage area

  • Monitor designated area with internet access lines and wireless connection.

  • Fully dedicated research facility equipped with exam/procedure rooms

  • ECG machines, centrifuge, copiers/fax machines.

  • Crash cart, oxygen, rescue medication

OFF-SITE

We have associate vendors for the bellow procedures:

  • Computed Tomography Scan (CT Scan)

  • Dexa Bone Density

  • EGD

  • FibroScan

  • Fluoroscopy

  • Magnetic Resonance Imaging (MRI)

  • Spirometry

  • Ultrasound

  • X-Rays

ON-SITE

Procedures we have experience performing at site:

  • ECG

  • GEBT

  • Insulin Titration

  • IV Infusion

  • Labs

  • Multiple Scales

  • PK

  • Satiety Test

  • Smart Pill

  • Spirometry

REGULATORY

Regulatory work and queries are typically taken care of within 24-48 hours
 

Our site recognizes the importance of timely start up and study related activities, the need to shorten
the time and expenses incurred in the whole process so our contract and budget are typically executed within 2 weeks of the documents receipt.

 

Most of our subjects are recruited from our site’s database and our investigators private practices,
consisting of thousands of potential patients that rely in our physician’s medical expertise, allowing us to be very successful at recruitment, compliance and retention with a very small screen failure rate.