Company Profile
Who is HRHR?
HRHR, Inc. is an independent, multi-therapeutic,
outpatient clinical research site located in Newport News, Virginia.
It
is conveniently located near I-64 and is 1.5 miles
from a local hospital. The 5,000 square feet research facility
is staffed
with full and part-time clinical research professionals.
The research professionals includes two Board Certified Physicians,
Certified Family Nurse Practitioners, registered
nurses and
Bachelor/Masters level employees with expertise in
conducting and facilitating clinical research studies. HRHR operates
according
to written SOPs and provides in-house training to all
employees.
Our site is affiliated with a large group of physicians with
a variety of backgrounds and specialties. These physicians
are Board Certified and have experience in clinical research.
Experience
HRHR, Inc. has conducted over 150 research studies and
has been a leading national enroller in a variety
of therapeutic areas since site initiation in 1998. Our research experience/interest includes Phase II, III, and
IV studies in the areas of:
Allergy
Hypertension
Cholesterol
Chronic Pain
Acute Infection
COPD |
Obesity
Asthma
Headaches
GERD
Gout
Diabetes |
Vaccine Research
Smoking Cessation
Irritable Bowel
Overactive Bladder
Depression
Osteoarthritis |
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.
More Information
on HRHR
|
