Research Center Profile:
Cardiology/Vascular Diseases
Scope of Services
Phase I
First Time in Man Safety/Tolerance
Bioavailability/Bioequivalence
Pharmacokinetics/Pharmacodynamics
Dose-Response
Drug Interactions
Metabolic Balance
Phase II-IV
Clinical Efficacy and Safety
Dose Ranging and Definition
Special Populations
Claims and Labeling Support
Post Marketing Studies
Rx to OTC Conversion
OCRC has expertise in evaluating products and conducting
research trials in the following areas of study:
Asthma
Anti-Infective (outpatient)
Analgesics
Bioavailability
CNS
Dermatology
Diabetes
Gastroenterology
Geriatrics
Hyperlipidemia
Hypertension
Nephrology
Nutrition
Pharmacokinetics
Psychiatry
Urinary Tract Infections
Weight Loss
Hormone Replacement Therapy
Smoking Cessation
Our streamlined and thorough planning, coordination and
monitoring process ensures both efficiency and exacting quality. At
OCRC we...
Enjoyed a close working relationship with IRBs so your research
protocol can be reviewed and implemented in a timely manner.
Appoint a coordinator who is familiar with every aspect of your
protocol to be a one-call source of information for you.
Support you in developing protocols by defining clinical
parameters.
Implement a recruiting and scheduling deadline that will meet
your milestone needs.
Provide outstanding patient care under the personal supervision
of Dr. Marbury.
Adhere strictly to all GCP and GLP guidelines.
Update your project daily and inform you quickly and accurately
about any adverse events.
Orlando Clinical Research Center (OCRC) is an independent Phase
I-IV custom built 35,000 SF research site specifically designed for
Phase 1 trials. The new facility includes 100 in-house volunteer
beds, dual lead digital telemetry, an upgraded security system with
card key access and digitally recorded cameras, as well as a
special treatment area with 12 hospital beds (6 of which are
plumbed for onsite hemodialysis).
100 beds for subject confinement
Separate accommodations for men and women
Recreational amenities:
Pool table
computer room with high speed and modem internet
connections
Direct TV
Cable TV in all rooms
VCR and DVD Players
24 hour medical coverage
Private Client Monitoring Room
12 exam rooms
Large special Treatment Lab with 12 hospital bed (6 are plumbed
for dialysis)
Certified sample processing laboratory
Freezers: 2 (-70°C) and 2 (-20 & C)
Refrigerated Centrifuge
Computerized EKG machines
Registered Dietitian Consultant
Orlando is one of the fast-growing cities in the U.S. and the
million-plus metro-area population encompasses all major
demographic groups for patient populations.
OCRC has a broad participant base that is continually augmented
and replenished by a highly successful recruiting program that taps
private practices and local hospitals, universities and retirement
communities.
Healthy volunteers
Hypertension
Diabetes
Renal Insufficiency
Elderly
Post-menopausal
Hepatic Dysfunction
Symptomatic Volunteers
Planning
In the initial phase of a project, OCRC will work with you to
ensure complete agreement as to a study's goals and its timely
completion. We can provide scientifically valid protocols, and
design original source documents to assure data accuracy and
facilitate information gathering.
Implementation
OCRC's experienced professionals provide rapid and accurate
data reporting and entry. We are time sensitive and have a record
of initiating studies within two weeks of final protocol and
Institutional Review Board (IRB) approval. OCRC utilizes multiple
FDA-inspected IRBs to assure that all protocols protect the rights
of clinical research subjects.
Reliable Data Information
We use both conventional CRF and remote data entry
simultaneously, so you may choose the method that works best for
you.
We also employ the latest data capture methods - including
scanned images/OCR - as well as traditional data transfer.
Most importantly, OCRC has received very satisfactory reviews on
audits conducted by our sponsors and by the FDA.
If you are interested in contacting this center to discuss placing a clinical
trial there, please complete and send the email form below. A representative from
the research center will then follow up with you.
