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Welcome to
Remington-Davis, Inc. Clinical
Research.
We are your source for
Clinically and Logistically complex
trials.
Experience Matters. Founded in
1992, Remington-Davis has grown into
a full-service, independent research
site conducting phase I-IV clinical
trials for the Pharmaceutical,
Biotech and Device industries. We
have completed over 350 trials in 18
therapeutic areas, including
critical care, emergency medicine
and trauma.
Housed in a 4,000 square foot
facility and partnering with 3 local
hospitals, you can be confident our
site has the capabilities and
experience to conduct your trial.
Your inpatient trial can draw from a
busy emergency room and over 2,223
inpatient beds across 3 hospitals.
Outpatient studies are performed in
our main office and satellite
offices, depending on your
requirements and expectations. Draw
from a robust subject database and a
combined statistical population of
1.98 million people.
Knowing that we have been audited
by the FDA and the European
Medicines Agency (EMEA), as well as
numerous sponsors, you can be
assured we have experienced, trained
and involved investigators working
on your study. Your CRA’s will
appreciate our large monitoring
areas, detailed source documents and
organized regulatory binders.
We are committed
to providing fast, accurate data by
having involved investigators,
dedicated study coordinators,
committed regulatory personnel and
knowledgeable support staff.
Our Values
We are committed to our values
both individually and as a team:
Maintaining the highest standards
of patient safety
Providing scientific information
that will improve healthcare for the
future
Earning respect and trust through
ethical behavior and honesty
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