From feasibility 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 profilesRequest access from our team. Approved sponsors receive a private access code with an expiration date. Do not share your code.
Request document accessThis restricted area uses an essential session cookie for up to 24 hours. Download activity is logged. Available documents depend on your authorization. Investigator summaries are based on October 2026 CVs; they are not substitutes for current signed CVs or credential verification. Current CVs, training and operational records must be provided and checked by the team. Expired documents cannot be downloaded.