Partner with MDC Clinical Research
We specialize in Phase II-IV clinical trials, providing end-to-end site management and execution services, including:
Rapid feasibility turnaround and protocol evaluation
Participant recruitment and retention strategies tailored to diverse populations
Electronic data capture (EDC) proficiency across multiples platforms
Strict adherence to ICH-GCP and FDA regulatory standards
Bilingual staff for broader participant engagement.
Therapeutic Experience
Our investigators and coordinators have conducted studies in:
Metabolic disorders ( Type 2 DM, Obesity and Lipid Management)
Gastrointestinal
Cardiovascular and Respiratory disease
Dermatology and vaccines
Women's health and Hormonal Therapy
Neurology and pain management.
Facility & Equipment
Our modern research center is designed for accuracy, safety and comfort:
Dedicated exam and procedure rooms
On site laboratory with refrigerated centrifuges ad sample storage
Temperature-monitored IP storage and accountability systems
ECG, spirometry and vital Signs monitoring
Emergency equipment and physician coverage
Secure electronic systems for source documentation and data management.
Performance Metrics
High enrollment-to-randomization conversion rates
Low screen failure and early withdrawal rates
Excellent monitor and sponsor feedback scores
Consistent audit-readiness and regulatory compliance.
Why Sponsors Choose Us
Experienced Principal Investigator: Dr Maria Curbelo Calleiro, MD with extensive clinical trial experience
Efficient Start Up: Rapid contract and regulatory submission turnaround times
Quality Data: Rigorous source verification and real-time query resolution
Strong Communication: Transparent, proactive updates for sponsors and CROs.
Let's Work Together
We welcome the opportunity to support your next clinical program.
Contact our Business Development team for feasibility request, site qualification, or additional information.
Phone: 305-425-1343
Email: mdcclinicalresearch@gmail.com