Phone (561) 816-2040 | Email info@prohealthresearchclinic.com | Location 3199 Lake Worth Rd. Suite A1, A2, A3, Palm Springs, FL 33461

Clinical Research Services

Full‑stack site support for Phase II–IV, devices, vaccines, and observational studies.

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What We Offer

Study Start‑Up

Rapid feasibility, site selection packages, IRB coordination, and contract/budget execution.

  • Feasibility & pre‑screening
  • Regulatory submissions
  • Contracts & budgets

Participant Recruitment

Community outreach, bilingual call center, and EMR‑assisted pre‑screens for qualified referrals.

  • Owned patient lists
  • Local media & outreach
  • Prescreen pipelines

Clinical Operations

GCP‑compliant visits with vitals, EKGs, labs, IP accountability, and deviation tracking.

  • PI/Sub‑I oversight
  • CRCs & RNs on site
  • 24/7 temperature logs

Data & Quality

eSource/ePRO ready, remote monitoring support, and 100% source‑to‑CRF verification.

  • EDC/ePRO/eSource
  • Query turnaround
  • Audit readiness

Safety Management

AE/SAE reporting, DSMB coordination, and secure PHI workflows aligned to HIPAA.

  • Real‑time AE capture
  • IRB & sponsor alerts
  • HIPAA‑compliant

Regulatory & Compliance

Robust SOPs, staff training, and version control for protocols, ICFs, and logs.

  • 21 CFR Part 11 ready
  • ICH‑GCP alignment
  • Inspection support

Therapeutic Areas

We collaborate with board‑certified investigators across multiple indications.

Cardiology Endocrinology Pulmonology Gastroenterology Dermatology Neurology Infectious Diseases Women’s Health

Our Study Process

1

Start‑Up

Feasibility, CTA/budget, and IRB submissions to launch on time.

2

Recruit & Enroll

Targeted outreach and prescreening to meet enrollment goals.

3

Execute Visits

Protocol‑driven procedures, IP control, and real‑time data entry.

4

Close‑Out

Query resolution, reconciliation, and inspection‑ready files.

Ready to Place a Study?

Send us your protocol synopsis or feasibility questionnaire. We’ll turn around quickly.

Contact Our Team