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Over 15 years of experience as a full-service CRO in Latin America. Conducted more than 70 clinical studies enrolling over 15,000 patients. Recognized for technical excellence and regulatory reliability. Fast-track regulatory approvals (2–3 months) and country start-up times (~5 months). Strong relationships with top-performing sites and patient organizations for rare diseases. All procedures are audited/certified for GCP compliance.
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