Overview

The Delaware Research Center was launched in 2005 as an offshoot of the research department of Family Practice Associates of Wilmington, Delaware http://fpade.familydoctors.net/. FPA has been performing clinical trials since 2000 with the help of two full-time clinical research coordinators, and a full-time clinical research assistant/patient recruiter. In addition to drawing patients from our six-clinician practice, we are also able to draw patients from the surrounding community via advertising and partnering with physicans in the greater Wilmington community.

Location

We are located at 1100 South Broom Street, Suite C, in Wilmington, Delaware, 19805. Our newly renovated office has a separate entrance with 2 fully equipped exam rooms, a room for monitors to use with high speed internet connections, a secured drug closet and refrigerator/freezer.

Staff

Ellen Neff, MSN Clinical Research Coordinator

Certified in Human Research Subjects Protection Training.

Lisa Romeo  Clinical Research Assistant, Patient Recruiter

David M. Krasner, D.O., FAAFP  Medical Director, Principal Investigator

Nine years experience conducting clinical research trials involving pharmaceuticals and medical devices. Dr. Krasner is an Associate Clinical Instructor at both Jefferson Medical College and the University of Delaware, and is a Fellow of the American Academy of Family Practice.

Edward R. Sobel, D.O.  Principal Investigator

Nine years experience conducting clinical research trials involving pharmaceuticals and medical devices.

Yvette Gbemudu, M.D.  Principal Investigator

Nine years experience conducting clinical research trials involving pharmaceuticals and medical devices.

All of our PI's are board certified in Family Practice, and are trained in Good Clinical Practices.

Other Information

  • We are able to utilize a central IRB and a central laboratory
  • Expedited protocol review, agreement, and budgeting
  • Expert subject recruitment and screening
  • Systems to ensure deadlines
  • Complete financial and administrative management
  • Full SOP and Quality Assurance systems
  • Strict compliance with FDA, GCP and ICH guidelines. 
  • Efficient sponsor-site communications and feedback
  • Excellent record-keeping and data integrity
  • Close oversight of protocol adherence
  • Performance milestone reports
  • Extensive experience in pharmaceutical and medical device trials

 

Questions or Comments: webmaster@deresearchcenter.com