Andes Clinical Research is proud of its highly skilled team, including a Principal Investigator and Sub-Investigators with over twenty years of combined experience in clinical research across various indications.

Our Principal Investigator always prioritizes patient safety and well-being.

Our research professionals, with a decade of clinical experience, are dedicated to maintaining data integrity. This commitment ensures we deliver high-quality, reliable, and safe outcomes in clinical research.

Streamlined and fully integrated operations for swift and efficient site selection.

Andes Clinical Research is committed to enhancing quality and efficiency in clinical trials.

Our rapid site selection, centralized communication, and streamlined processes ensure a fast turnaround for contract and budget responses (48-hour turnaround for contract/budget responses).

With a single contact point, we provide seamless trial management.

Andes Clinical Research, with precision design, ensures accurate enrollment and retention for challenging research programs.

Our experienced recruitment team continuously enhances processes for recruitment, screening, and retention.

We maintain an updated list of prospective participants ready for screening upon activation.

Key features include proprietary databases, rapid enrollment support, robust community outreach, and advertising solutions.

Andes Clinical Research establishes an industry-leading quality oversight model, leveraging internal teams in clinical data, quality assurance, regulatory, and risk management.

Seasoned experts working to ensure trial success, acting as valuable resources for continuous improvement. Their support ensures adherence to FDA regulations, ICH GCP Guidance, state guidelines, industry standards, and Andes Clinical Research's rigorous SOPs.

Key features include a timely query resolution, routine QA reviews, commitment to training, and certified labs and staff for comprehensive quality assurance.