IQVIA is the world's largest CRO and healthcare-data company, with global reach across every phase, therapeutic area and post-market service. It's a strong choice for large sponsors that need scale, real-world evidence and integrated commercialization. bioaccess® is the First-in-Human CRO — built for the U.S. and Latin America — and only runs FIH studies for startups. If the next milestone is a clean, FDA-bridgeable first-in-human dataset on a startup timeline, bioaccess® is purpose-built for it.
| Metric | bioaccess® | IQVIA |
|---|---|---|
| Focus | FIH-only for MedTech, Biopharma & Radiopharma startups | Full-service global CRO — all phases (I–IV), all therapeutic areas, all sizes; FIH is a small slice of the portfolio |
| Footprint | U.S. + 10 Latin American countries, 50+ pre-qualified sites | Global (50+ countries) — strong in U.S., EU, and APAC |
| Typical ethics / IRB timeline | 4–8 weeks (Latin American ethics committees) | 6–12 months typical in US/EU jurisdictions |
| Typical per-patient cost | $15K–$35K | $40K–$75K in US/EU benchmark ranges |
| FIH start (protocol → first patient) | 6–8 weeks via FIH FastTrack | Category benchmark: 6–12 months for large global CROs running FIH inside US/EU networks |
| Pricing model | Fixed-price with 12-month risk-sharing guarantee — we work at our cost if we miss agreed milestones | Typically time-and-materials or milestone-based; category norm includes change orders |
| Regulatory standard for devices | ISO 14155 + Declaration of Helsinki; data eligible for FDA submission/review under 21 CFR 812.28 | ISO 14155 and ICH E6 GCP; broad regulatory coverage worldwide |
| Best-fit sponsor profile | Seed-to-Series-B MedTech, Biopharma & Radiopharma startups running their first FIH study | Mid-to-large pharma/medtech running pivotal, registration, or post-market programs across regions |
| Post-trial support | Latin American market access, device registration in 10 countries, HTA & payer engagement | Extensive commercialization, real-world evidence and pharmacovigilance services worldwide |
Comparison uses widely-known category facts about IQVIA and published US/EU benchmark ranges — not IQVIA-specific figures. bioaccess® figures reflect our FIH FastTrack operating model.
IQVIA is a category leader for exactly the sponsors it was built for: mid-to-large biopharma and medtech running large, multi-region programs where scale, data assets and integrated commercialization are the deciding factors. Those advantages don't compound as strongly on a single-site, 10-patient first-in-human study.
bioaccess® is built for that first-in-human job specifically. FIH-only. Startup-only. U.S. regulatory anchoring plus Latin American execution. That focus is what lets us commit to a 6–8 week study start, 4–8 week ethics approval, $15K–$35K per patient, and a 12-month protocol-to-LPLV written guarantee — with a risk-sharing clause that keeps us working at our cost if we miss an agreed milestone.
Data is generated under ISO 14155 and the Declaration of Helsinki and is eligible for FDA submission and review under 21 CFR 812.28 (for devices) or ICH E6 for drugs and biologics — a case-by-case regulatory determination, not a guarantee of clearance or approval. The FIH package is designed to hand off cleanly to any downstream CRO — including IQVIA — for a pivotal or registration program.
Only in a narrow slice. IQVIA is a large, reputable organization serving a broad customer base across many programs. bioaccess® is purpose-built for a single job: first-in-human clinical trials for MedTech, Biopharma and Radiopharma startups, executed across the U.S. and Latin America. If your program is a global pivotal or a post-market study, IQVIA is often a better fit. If your program is your first-in-human trial and you need clean, FDA-bridgeable data on a startup budget and timeline, bioaccess® is purpose-built for it.
Clinical data from studies conducted outside the U.S. under ISO 14155 and the Declaration of Helsinki is eligible for FDA submission and review under 21 CFR 812.28 (for devices) and comparable ICH E6 pathways for drugs and biologics. Acceptance is a case-by-case regulatory determination, not a guarantee of clearance or approval — our regulatory team designs the study with the target FDA submission (IDE, 510(k), De Novo, PMA, HDE, IND) as the anchor.
A standard 10-patient, single-site FIH study through FIH FastTrack runs roughly $350K all-in, with a 12-month protocol-to-LPLV written guarantee and a 6–8 week study start. Per-patient cost is $15K–$35K vs. $40K–$75K in US/EU benchmark ranges. Ethics approval is 4–8 weeks in Latin American jurisdictions vs. 6–12 months in the US/EU.
Yes — sponsors regularly do. A common pattern is to run FIH with bioaccess® in Latin America to generate clean, regulator-ready data fast, then hand off to IQVIA (or a similar global CRO) for a multi-region pivotal, registration, or post-market program. Our regulatory strategy is designed to be portable so that data and documentation transfer cleanly to any downstream CRO.
No — that's not our scope. bioaccess® is focused on first-in-human clinical execution across the U.S. and Latin America, plus Latin American market access and device registration. For large-scale real-world evidence programs or global healthcare-data analytics, a data-centric organization like IQVIA is a better fit. The two are complementary: run FIH with bioaccess® to generate clean, regulator-ready data fast, then use an IQVIA-class partner for downstream evidence generation at scale.
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