Community-Based Clinical Research, Built for Sponsors and Patients.

AME Clinical Research partners with sponsors and CROs to conduct high-quality internal medicine and geriatric clinical trials in a diverse South Florida patient population.

AME Clinical Research partners with sponsors and CROs to conduct high-quality internal medicine and geriatric clinical trials in a diverse South Florida patient population.

Therapeutic Focus & Site Capabilities

Focused internal medicine and geriatric research with access to diverse, treatment-naïve patient populations in South Florida.

Focused internal medicine and geriatric research with access to diverse, treatment-naïve patient populations in South Florida.

Focused internal medicine and geriatric research with access to diverse, treatment-naïve patient populations in South Florida.

Therapeutic Focus

Internal Medicine

Experience supporting clinical trials across chronic conditions commonly seen in internal medicine, including cardiometabolic, renal, and age-related diseases.

Patient Population

Geriatric Research

Dedicated access to older adult populations through an established geriatric practice, supporting studies requiring consistent follow-up and long-term care insight.

Why Sponsors Work With AME Clinical Research

Established Patient Access

Embedded within an active internal medicine and geriatric practice, providing consistent access to treatment-naïve and follow-up-ready patients.

Operationally Ready Site

Startup site built with sponsor expectations in mind, including regulatory readiness, dedicated research workflows, and rapid activation timelines.

Diverse South Florida Population

Located in Miramar, Florida, serving a highly diverse patient population supportive of inclusion and diversity enrollment initiatives.

Regulatory Compliance & Data Protection

Regulatory Compliance & Data Protection

Regulatory Compliance & Data Protection

AME Clinical Research operates under strict regulatory and data protection standards to ensure subject safety, data integrity, and sponsor confidence.

HIPAA & 21 CFR Part 11 Compliance

All study data is handled in accordance with HIPAA regulations and 21 CFR Part 11 requirements, ensuring confidentiality, audit trails, and secure electronic records.

IRB Oversight & GCP Standards

Studies are conducted under Institutional Review Board (IRB) approval and in compliance with ICH-GCP guidelines, supporting ethical conduct and high-quality clinical outcomes.

Start a Feasibility Discussion With AME Clinical Research

Start a Feasibility Discussion With AME Clinical Research

Start a Feasibility Discussion With AME Clinical Research

We welcome early feasibility conversations with sponsors and CROs seeking high-quality internal medicine and geriatric research sites in South Florida.