Why Innovators Choose bioaccess®’s Global Network
Latin America
- Speed: Panama, El Salvador, Chile approvals in 4-8 weeks vs. 6+ months in US/EU.
- Cost: $25K/patient savings with pre-negotiated site contracts.
- Post-Trial Edge: Fast-track commercialization in LATAM's $1.2B MedTech market.
Eastern Europe
- Parallel Reviews: Ethics + ALIMS approvals in 80 days via Serbia’s ADIS portal.
- Diverse Populations: Rare disease cohorts in Kosovo; cardiology KOLs in Belgrade.
- EU Gateway: CTR-aligned data for seamless EMA submissions.
Australia
- CTN Speed: TGA acknowledgment in 5–10 days for low-risk trials.
- ICH-GCP Compliance: 100% FDA/EMA acceptance with no data rework.
- Strategic Bridge: Run Phase I trials while preparing US IND.
Digital Health Startup CEO
"bioaccess®’s Serbia site activated in 8 weeks-9 months faster than our EU delay.”
Services
End-to-End Acceleration for Global Trials
Regulatory Sprint
Parallel submissions in LATAM, Balkans & Australia
Patient Recruitment at Warp Speed
Pre-qualified networks: 50+ sites activated in <8 weeks.
Site Activation in <8 Weeks
FDA/EMA/MDR-ready datasets with centralized monitoring.
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Unlike generic CROs, bioaccess® combines regional speed/cost advantages with deep regulatory expertise to de-risk trials for startups prioritizing time-to-market and investor-ready outcomes.
Trusted by
Committed To Your Success
bioaccess® is a US-based CRO that bridges the gap between innovative Medtech and Biopharma companies and the untapped potential of conducting clinical research studies in Latin America.
Our team believes in the importance of your medical device and the benefit it could bring to people’s lives.
We are committed to helping you navigate the convoluted and uncertain developmental challenges of being an early-stage startup. Our priority is bringing you fast, cost-effective, and high-quality clinical data.
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