Feasibility questionnaires are turned around in 48 hours or less. Providing historical enrollment metrics allows feasibility and site identification to occur at an accelerated pace. In order to help our sponsors, reduce study start up timelines, ICR offers a more proactive, streamlined approach to the negotiating process. Contract and Budget Negotiations within 2 weeks whiles we begin the IRB process.
BCR database includes metrics from PIs and Sub-I(s). This diverse database gives us the ablility, to forcast and plan enrollment, focus on required demographics of each protocol.
Discover Biscayne Clinical Research
Step inside a center where medical advancement meets human connection. Our virtual tour takes you behind the scenes to see how we turn groundbreaking studies into real-world care.
• A modern 8,000-square-foot facility built for precision and patient comfort
• Specialized spaces for exams, infusions, monitoring, and secure medication management
• A welcoming atmosphere designed to make every visit safe, efficient, and stress-free
At Biscayne Clinical Research, every detail supports one goal. Advancing health through innovation and trust for everyone.
Yes, you can. To participate in a given study you must qualify by meeting the research criteria. Eligibility can be determined by good health or specific medical diagnosis, as well as age, gender, and current medication.
Volunteering contributes to the advancement of medical knowledge and treatments.These Trials carefully designed medical activities that allow the evaluation of safety and efficacy of new medication
We look forward from hearing from you. Send us a message today.