Services

Our focus is on delivering the highest quality service through our commitment to rapid enrollment procedures, quality data collection and patient safety. HRHR has brought together a team of clinical research professionals committed to a single focus - study conduct and outstanding performance records in a wide variety of therapeutic areas. We are the experts in recruiting patients, executing studies and collecting data.

Who is HRHR?

Health Research of Hampton Roads, established in 1998, is a privately owned clinical research facility dedicated to the development of new and advanced treatments for common medical problems.

All of the clinical trials at HRHR are carefully controlled studies of investigational treatments. These studies are regulated by the Food and Drug Administration (FDA) and are overseen by a board-certified physician.

The physician is assisted by highly trained and experienced, certified clinical research professionals that are committed to the shared goal of advancing the search for better health through the discovery of new therapies.

Therapies for a number of medical problems are ongoing and may include investigational treatments for:

Our Commitment

By combining the talents of experienced investigators and research coordinators we have become the experts in:

Service: Through our single focus, the conduct of clinical trials, we are able to uniquely provide to each patient/subject a greater degree of personal attention from not only coordinators, but from investigators as well. Likewise, Sponsors/CROs benefit from ready access to an investigator that is consistently on-site. As a privately owned, multi-therapeutic, dedicated research investigative site, HRHR assures a high quality consistency of purpose by devoting attention solely to patient safety, high enrollment and quality data management.

Performance: Repeatedly meets and exceeds client expectations, frequently exceeding enrollment goals and ranking nationally in the number of evaluable patients.

Reliability: Recognizing that poor data, regardless of enrollment numbers, negates the value of the research trial for the sponsor as well as the patient, HRHR starts each study recognizing and targeting the study objectives and endpoints. We then strive to meet study objectives by obtaining objective and true measurements.

Recruitment: Research personnel dedicated to innovative patient recruitment practices.

IRB Approval: HRHR prefers utilization of multiple central IRBs in its approval process resulting in faster study initiation.

Project Management: Privately owned facility with streamlined process to negotiate contracts and budgets. Trial management teams conduct each trial to assure superior recruitment and data management.