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Boutique CRO · Monterrey, México

Your LATAM
Clinical Trials Ally

Find solutions. Make them happen.

Clinical Trial Management · Regulatory Affairs · Pharmacovigilance · Early-Phase Trials · Data Management · Site Monitoring & Auditing · Real World Evidence · Clinical Trial Management · Regulatory Affairs · Pharmacovigilance · Early-Phase Trials · Data Management · Site Monitoring & Auditing · Real World Evidence

Built on experience.
Driven by commitment.

Althian is a boutique Contract Research Organization based in Monterrey, México, supporting pharmaceutical, biotechnology, and medical device sponsors with clinical trials in Mexico and Latin America. We combine 15+ years of on-the-ground experience with local regulatory expertise and the personalized attention only a boutique CRO can offer.

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Our Services

Clinical Trial
Management
End-to-end study coordination: site selection, patient recruitment, monitoring, and final reporting across Mexico and LATAM.
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Regulatory Affairs
Full regulatory submissions and dossier preparation to support your clinical trial approvals in Mexico and LATAM.
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Early-Phase Trials
Phase I/II studies including bioavailability and bioequivalence, supported by experienced clinical operations teams.
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Pharmacovigilance
& Safety
Continuous adverse event monitoring, safety reporting, and post-approval lifecycle management aligned with global standards.
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Data Management
Robust data collection, cleaning, and analysis frameworks ensuring integrity and reliability of your study results.
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Real-World Evidence
Post-marketing surveillance and observational studies generating actionable insights from real patient populations in LATAM.
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Why Althian

A partner who will treat your study as their own

We combine local regulatory expertise with the operational agility and personalized attention that only a boutique organization can offer.

Built from site experience

We spent 15+ years on the ground before becoming a CRO. We know what investigators need, what sponsors expect, and where things go wrong.

Boutique means you matter

No black holes, no junior handoffs. You get direct access to the people actually running your study.

Local expertise, global standards

COFEPRIS submissions, Ethics Committee management, and ICH-GCP compliance — all handled in-house.

Why Althian

Ready to bring your study to LATAM?

Tell us about your project. We'll make it happen.

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