(561) 816-2040
|
info@prohealthresearchclinic.com
|
3199 Lake Worth Rd. Suite A1, A2, A3, Palm Springs, FL 33461
(561) 816-2040
|
info@prohealthresearchclinic.com
|
3199 Lake Worth Rd. Suite A1, A2, A3, Palm Springs, FL 33461
Pro‑Health Research Clinic is a dedicated clinical research center in Palm Springs, Florida. We partner with patients, sponsors, and CROs to conduct safe, ethical studies that advance healthcare while delivering respectful, high‑quality care.
To advance medical knowledge through high-quality clinical research while prioritizing patient safety, comfort, and trust.
To be a leading research clinic in South Florida, recognized for innovation, integrity, and compassionate patient care.
Our site is equipped to run Phase II–IV studies with strict adherence to Good Clinical Practice (GCP) and patient safety.
Principal Investigator, Sub‑Is, CRCs, and RNs with therapeutic‑area experience.
Vitals, phlebotomy, EKG, sample processing, and temperature‑controlled storage.
HIPAA‑compliant workflows, privacy‑first intake, and bilingual staff (EN/ES).
IRB oversight, SOPs, deviation tracking, and 100% source‑to‑CRF verification.
Community outreach, pre‑screen pipelines, and EMR‑assisted eligibility checks.
eSource/ePRO ready, GCP/ICH‑aligned, and sponsor audit support.
We partner with sponsors and CROs across multiple indications and phases.
Clinical research helps bring new treatments to life. At Pro-Health Research Clinic, your safety and comfort come first, and participation is always voluntary.
Study-related exams, labs, and procedures are provided at no cost to you.
Eligible participants may receive compensation for time and travel.
Our licensed medical team follows IRB-approved protocols and GCP standards.
Brief call and eligibility questions. We review medical history and answer questions.
In-clinic visit for consent, vitals, and any study-related tests or procedures.
Ongoing check-ins to monitor health, with clear guidance at every step.
Have questions about study participation? Here are the basics. If you don’t see your question, contact us—we’re happy to help.
Safety is our top priority. All studies follow IRB‑approved protocols and Good Clinical Practice (GCP). You’ll review an informed consent form and can ask questions before any procedures begin.
No. Study‑related exams, labs, and procedures are provided at no cost. Many studies also offer compensation for time and travel if you qualify.
Participation does not replace your regular medical care. Study‑related costs are covered by the study. Your personal information is protected under HIPAA.
Yes. Participation is completely voluntary. You can withdraw at any time, for any reason, and this will not affect your future medical care.
It varies by study. Screening visits can take 30–90 minutes; study visits may take longer depending on the procedures required. We’ll tell you the expected time before you come in.