Principal Investigator
Orlirio Corrales, MD
Internal medicine, hospital care and clinical teaching. A clinical perspective on participant assessment and medical oversight.
English · SpanishIHR / The sponsor studioHialeah · South Florida
Your protocol.
Our people.
Let’s talk.
A closer look at the people, spaces and conversations behind Integrated Health Research. Built for a thoughtful site evaluation.
Our published study scopePhase II–IVOutpatient research. Human connection.
Integrated Health ResearchActual site photography
01 / An open doorSee the place.
See the place.
Picture the conversation.
Select a space to explore photographs from our actual center. Then come see it with your team.
Photography shows the center as documented. Equipment suitability, monitoring, access and space allocation are reviewed for each protocol.
02 / People behind the protocolClinical perspective.
Read the investigator profiles ↗Clinical perspective.
A personal introduction.
Sub-Investigator
Natalia Escuti, MD
Family medicine and clinical trial operations. Experience spanning study startup, monitoring and closeout.
English · Spanish · FrenchProfiles are based on physician-provided CVs. Current qualifications, training and availability are confirmed during protocol-specific review.
03 / Start with your studyYour protocol.
Your protocol.
A more focused
first conversation.
A few details turn into a clear discussion brief. Explore what to review, then bring it to our team.
04 / Make the next step countA clear starting point.
A clear starting point.
Evidence for
your evaluation.
Take the overview with you. Review the published capabilities. Request the documentation your team needs.
Integrated Health Research / HialeahThe right questions
The right questions
deserve a conversation.
Let’s explore your protocol, your requirements and the next step together.
Before you send a protocol
Start with nonconfidential study requirements. Agree confidentiality terms with the team before sharing a confidential protocol. Our published scope is Phase II–IV outpatient research, without overnight stays. Enrollment, readiness and study approval require a specific assessment.
From first contact to site qualification
Share your study requirements
Send the phase, indication, enrollment target, timeline and visit requirements through the sponsor form. Phase II–IV only; do not attach patient information.
Arrange confidential document review
Discuss confidentiality requirements with the team before sharing a confidential protocol. Authorized sponsors can receive a private, expiring document-access code.
Complete site qualification
Coordinate a visit to review investigator availability, equipment suitability, operational records and protocol requirements. A requested visit is subject to confirmation.
Confirm readiness before activation
The sponsor and site must resolve open requirements and confirm applicable approvals, agreements and protocol-specific readiness before study activities begin. A web inquiry does not activate a study.
Investigator profile sources and verification
Investigator profile sources: CVs dated October 5, 2026 for Orlirio Corrales, M.D. (Principal Investigator) and Natalia Escuti, M.D. (Sub-Investigator). These are profile sources, not a current credential verification. Request signed CVs and up-to-date licenses and training records from the team. Investigator experience does not establish completed studies or performance at IHR.
View investigator profilesQuality evidence for your review
Use this checklist to request and verify evidence with the team. Listed documents are review requirements; listing them does not confirm that each has been uploaded or validated.
Authorized scope
Phase II–IV, outpatient; no Phase I or overnight stays.
Review applicable authorization and protocol-specific approvals.
Investigator qualifications
Investigator profiles and a private document center are available.
Request current signed CVs, licensure and training records.
Equipment suitability
Reported units: −80°C, −40°C and +20°C.
Review inventory, actual settings, calibration, monitoring and contingency records.
Clinical quality processes
To be reviewed during site qualification.
Request applicable SOPs, delegation, safety escalation, source documentation and data quality procedures.
Inspection / performance history
No inspection outcome or site performance statistic is asserted here.
Request documented history when available; distinguish investigator experience from site results.