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Monday – Friday : 9:00am – 5:00pm
Saturday & Sunday : Closed

SPONSORS & CROs

Our team efficiently completes all stages of awarded Clinical Trials. From feasibility review to close out diligence, our integrated electronic systems facilitate an almost complete paperless trial execution. Our processes and systems allow user-friendly remote data verification and monitoring.

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For Sponsors

CTMD Research is an independent clinical research facility that executes high-quality research studies for pharmaceutical companies and clinical research organizations in Central Palm Beach County, and Broward County, Florida, USA.

  • Specializing in Family Medicine
  • Expertise across various health conditions, and studies involving healthy volunteers
  • Extensive experience spanning Phase 1 to Phase 4 trials
  • Outpatient trials utilizing Central Institutional Review Boards (IRBs)
  • Efficient study start-up, with an average time from Study Award to Site-Initiation readiness of fewer than 2-4 weeks
View Our Therapeutic Expertise

For CROs

We streamline the clinical trial recruitment processes, expediting your organization’s expansion into new markets and therapeutic areas.

  • Site management expertise
  • Minimizes recruitment timelines
  • Maximizes enrollment success
  • Efficient data-driven recruitment strategies
View Our Therapeutic Expertise
FAQ’s

Frequently Asked
Questions

How does your CRO ensure quality and compliance throughout the research process?

We maintain strict adherence to regulatory requirements and industry standards, conducting regular audits and implementing robust quality control measures at every stage of the research process. Our team is trained in Good Clinical Practice (GCP) guidelines and is committed to upholding the highest standards of quality and compliance.

How do you handle data management and ensure data integrity?

We have robust data management systems and processes to ensure study data’s accuracy, completeness, and integrity. Our team is experienced in data collection, cleaning, and analysis, and we adhere to stringent data security protocols to protect sensitive information.

How does your CRO ensure patient safety and regulatory compliance?

Patient safety is our top priority, and we adhere to all applicable regulatory requirements and guidelines to ensure the ethical conduct of clinical trials. Our team conducts regular site visits and monitors patient safety data closely to identify and mitigate any risks to participants.

Contact Us

Reach out to us for a consultation to explore which clinical trials may be suitable for your needs.

Want to get involved?