Quality Research of South Florida is a private Clinical Research Site based in Miami Lakes, Florida. The Research Director founded our organization in June 1999. With over 25 years of research experience is currently dedicated to advancing health of our community through advances in medical research.

As a privately owned facility, we continue to grow and expand our specialties, bringing more Board-Certified Cardiologists, Allergists, Internal Medicine, OBGYN, Family Practice, Hematologists and Pain Management practitioners to our team. We offer unique and highly effective investigative site for conducting Phase II-IV Studies for a wide range of therapeutic areas.

Quality Research of South Florida Facility
Located in center of Miami city of Miami Lakes, Quality Research of South Florida has 3,100 square feet of dedicated clinical research space. The center is approximately 20 minutes North from Miami International Airport and approximately 20 minutes South of Fort Lauderdale Airport in Miami; We are fully equipped to conduct Phase II-IV trials. (Able to accommodate subjects for a 12-24 hours stay clinical trials.)

Equipment/Facility
• Access to Beds
• -20° Freezer
• Electrocardiogram Machines
• Digital Vital Signs Monitors
• Fully equipped Laboratory
• Refrigerators for specimens
• Refrigerated Centrifuges
• Pharmacy/Drug Storage Room with refrigerator
• Conference Room
• Monitoring Rooms
• Patient Examination Rooms
• Outpatient/Screening Area
• 12 lead EKG
• Biofeedback
• Centrifuges
• CLIA
• Dry Ice
• Uroflowmetry
• Ultrasounds
• Spirometry

We have access to many other diagnostics such as:
• Bone Mineral Density- DEXA scan
• CT Scan
• Diagnostic X-Ray
• Mammography
• MRI

Other features within Quality Research:
• 24 hour emergency phone number
• Computerized software for daily tracking of patient activity
• Standard Operating Procedures
• QA audit tools and procedures for FDA compliance
• Competency documentation tools for clinical trials staff
• Training in the clinical trials industry (GCP & ICH) and FDA regulations for clinical trials staff
• IATA Certified staff
• Human Participant Protections Education for all Staff
• Ongoing review of clinical trial regulations and system adaptation
• Prompt turn-around of regulatory documents, contracts, and budgets
• One person contact for all study-related issues
• Subject recruitment plan and execution
• Computerized software for daily tracking of patient activity
• Accurate results in a timely manner with data integrity
• Well trained coordinator staff
• Large detailed database subdivided to recruit subjects
• Use of a central IRB which facilitates timely approvals
• Demographically, ethnically diverse patient population
• High speed internet access with wireless capabilities
• High enrollment of past studies
• Open evenings and weekends as needed

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