For sponsors and CROs

The #1 reason trials slip is recruitment. It is the thing we are built for.

A dedicated clinical research center in Tampa Bay, staffed by Clinical Research Coordinators (CRCs) who are International Medical Graduates (IMGs), supported by an in-house Regulatory Affairs Department, an established patient referral network, and a proactive communication culture committed to responding to clinical research monitor inquiries on the same business day.

Un centro de investigación clínica especializado en Tampa Bay, con Coordinadores de Investigación Clínica (CRCs) que son Médicos Graduados Internacionales (International Medical Graduates – IMGs), un departamento interno de asuntos regulatorios, una sólida red de referencia de pacientes y una cultura de comunicación proactiva, comprometida con responder las consultas de los monitores de investigación clínica el mismo día.

Request feasibility
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From synopsis to first patient in

Typical timeline for a central-IRB study once the CDA is countersigned. Local requirements can shift individual steps; the order does not change.

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Since 2021

Who we work with

What we study

Therapeutic experience

Open to new indications where the Tampa Bay population and our referral network support enrollment.

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At a glance

Site facts

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Request feasibility.

Fast Track option available. After receiving, revision and signing of the CDA/NDA, please send the synopsis or protocol number. We respond with eligible-population estimates, competing-study status and a realistic monthly enrollment rate for this site.

Thank you. A study coordinator will reply within two business days.
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