Clinical research in the Western Amazon
IPES gives sponsors and CROs access to a patient population that rarely appears in global trial data — with ICH-GCP standards, a dedicated team and hospital-based infrastructure in Porto Velho.
Why run a study with IPES
What a site in Rondônia offers that a site in São Paulo or Rio does not.
A population that is genuinely treatment-naïve
Rondônia sits outside Brazil’s established research corridor. Patients here have had far less exposure to investigational products and to competing trials, which shows up directly in eligibility rates and in the cleanliness of your data.
Low competition for participants
Fewer active sites in the state means less recruitment overlap. Your study is not competing with three others for the same patients in the same waiting room.
Inside a working hospital
IPES operates within Hospital ProntoCordis, so cardiology, imaging, laboratory and emergency support are in the same building — not scheduled across town.
Built for regulated research from day one
Ethics review through Brazil’s CEP/CONEP system, ANVISA-regulated procedures, ICH-GCP-trained staff, and traceable participant data with LGPD-compliant handling.
Considering a site in Brazil?
Send us your protocol synopsis and we will come back with a realistic feasibility read — including what we can and cannot recruit for. We would rather decline a study than miss enrolment targets.