For Research Sites & Partners

Partner with our Principal Investigator

A GCP-current, ICH-GCP Principal Investigator available to lead trials for research sites and networks/SMOs across South and Central/West Coast Florida. Sponsors and CROs seeking an investigator in these regions are welcome too.

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PI availability

A credentialed Principal Investigator available to lead trials at your site or across your network — dual-region coverage in South and Central/West Coast Florida.

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Oversight scope

Direct PI oversight of protocol conduct, subject safety, and regulatory responsibilities (FDA 1572), grounded in ICH-GCP.

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Confidential by default

Oversight terms, capabilities, and operational detail are shared under a confidentiality agreement — not published.

Feasibility process

Share your indication and protocol parameters; we assess fit against the PI's experience, your population, and our capabilities, then return a confidential feasibility response.

Confidential intake

Tell us about your site and the study. We'll follow up to coordinate a CDA before exchanging specifics.

By submitting, you consent to RenuviaMD PLLC contacting you about your inquiry. Do not include confidential or protected information in this form; specifics are exchanged under a confidentiality agreement.

Thank you. If you've just submitted the form, we've received your inquiry and will follow up to coordinate a confidentiality agreement before exchanging specifics.