Welcome to CDL Research Institute
FOR SPONSORS & CROs
A Research Site Focused on Quality, Responsiveness & Reliable Study Execution
CDL Research Institute partners with pharmaceutical sponsors, biotechnology companies, medical device developers, and Contract Research Organizations (CROs) to support the execution of clinical research in a multidisciplinary outpatient medical environment. Our approach emphasizes participant safety, protocol compliance, data quality, responsive communication, and reliable study operations.
Site Capabilities
- Study feasibility and site qualification support
- Participant identification, pre-screening, recruitment, and retention support
- Protocol-driven participant visits and clinical assessments
- Source documentation and study record management
- Regulatory document support and study start-up coordination
- Sponsor and CRO monitoring support
- Safety reporting and protocol compliance support
- Study-specific investigational product handling and storage when required capabilities are verified and activated
- Coordination of protocol-required diagnostic and clinical services when available and appropriate
Why Partner With CDL Research Institute?
Located in Doral within the greater Miami-Dade region, CDL Research Institute combines multidisciplinary clinical expertise with a patient-centered research environment. Our team evaluates each study opportunity based on investigator experience, protocol requirements, available patient populations, operational readiness, and the site’s ability to execute the study responsibly and efficiently.
Therapeutic Areas of Interest
- Pain Medicine
- Musculoskeletal & Spine Disorders
- Osteoarthritis & Joint Disorders
- Neurology & Neurosciences
- Neuropathic Pain
- Rehabilitation & Recovery Medicine
- Medical Device & Digital Health Research
Quality, Compliance & Participant Safety
Our research operations are designed to support Good Clinical Practice (GCP), protocol adherence, Institutional Review Board (IRB) requirements, accurate source documentation, participant safety, data integrity, and responsive sponsor/CRO communication. Study-specific regulatory and operational requirements are reviewed during feasibility and study start-up.
Sponsor & CRO Collaboration
CDL Research Institute is committed to timely communication with sponsors, CROs, monitors, and study teams throughout study start-up, enrollment, conduct, monitoring, and close-out. Monitoring arrangements and access to study documentation are coordinated according to protocol, sponsor, regulatory, and privacy requirements.
Multidisciplinary Research Team
Our research environment is supported by physicians, advanced practice providers, and clinical support professionals whose participation is assigned according to each protocol, investigator qualifications, delegation requirements, and applicable scope of practice. Investigator and staff credentials should be provided to sponsors and CROs as part of feasibility and site qualification.
Discuss a Clinical Trial Opportunity
