ABOUT US
We are experts in delivering cost-effective and high-quality CRO services in Latin America. We partner with Medtech startups seeking accelerated early-feasibility (EFS) or first-in-human (FIH) clinical study results. With bioaccess™, you quickly and reliably receive regulatory approval, clinical research site activation, subject recruitment, and clinical trial data.
Why Colombia?
Imagine if you could conduct your early-feasibility (EFS) or first-in-human (FIH) clinical study on a +52-million-people country with 99% of its population covered by a top-performing universal healthcare system; with a 30-90 day national Ministry of Health (MoH) evaluation timeline for clinical trials; with OECD membership that ensures alignment of its legislation, policies, and practices to global first-world standards; and with a free-trade agreement with the US. Read more.
Team
bioaccess™ has an expert clinical research team. It includes members with over +20 years of proven experience in Latin America. They have processed and approved hundreds of regulatory dossier files in Latin America for first-in-human and early-feasibility studies.
First-In-Human Clinical Trials, Regulatory Affairs, Distributor Search in Latin America