Delta Research Partners is built on a commitment to conduct clinical trials using the highest standards of ethics to contribute in the development of safe and beneficial medical products. We bring innovative research to the Delta.

elta Research Partners was founded in 2003. Located in Monroe, Louisiana, Delta is an independent research center dedicated to conducting high-quality clinical research trials in multiple therapeutic areas. Delta has a strong network represented by our Principal Investigator and several Sub-Investigators, all board-certified in Internal Medicine and Gastroenterology.  Our team is lead by Principal Investigator, Dr. Raj Bhandari, who is triple-board certified in Internal Medicine, Gastroenterology, and Nutrition.

Our Mission:

  • To provide a comprehensive set of services to aid in the process of bringing new effective treatments to the market, through Phase II, III, and IV clinical trials. We also have experience with Phase I studies.
  • Committed to conducting clinical trials using the highest standards of ethics.
  • Strive to assist the trial sponsors in meeting and exceeding their subject recruitment goals
  • Assuring high quality data is collected throughout the trial process.

Delta is located in Northeast Louisiana with an estimated 350,000+ population in our community and surrounding areas. Our own database consists of over 100,000 subjects. We also have an extensive referring physician database with over 350 physicians that are a great source to our subject recruitment. The physicians are from various specialties including:

  • Gastroenterology/Hepatology
  • Family Medicine
  • Internal Medicine
  • Pain Management

Delta is committed to assisting physicians and their subjects to having access to new and promising treatments that can improve quality of life. Our community has a positive attitude toward research and we are able to generates a tremendous response with the use of IRB approved ads and flyers.

Delta is affiliated with two independent Gastroenterology Practices in Northeast Louisiana and an Ambulatory Surgery Center (ASC). Since we have two (2) separate study sites (Monroe & Bastrop), monitors can monitor two different sites with one visit.

Note to Clinical Research Organizations:

  • CTA/Budgets and Contracts will be completed expeditiously.  We have no bureaucracy within our organization and are able to complete documents quickly. We guarantee to return all study documents within 48-72 hours.
  • We utilize the IRB of your choice or a central IRB for efficiency. We do not use a Local IRB.