Nivella

Nivella Health is a Clinical Research Organization (CRO) and Site Management Organization (SMO) providing cost-effective, high-quality clinical trial execution for biotech, pharmaceutical, and CRO sponsors. Based in Rwanda, we deliver fast, globally compliant research solutions that reduce costs, accelerate timelines, and ensure FDA/EMA-ready data. With a WHO Level 3–recognized regulatory framework, one of Africa’s fastest approval timelines (as little as 2 months), and a 150,000+ patient database, Nivella enables sponsors to launch trials faster, enroll patients more efficiently, and cut trial costs by 50% or more. Why Nivella? ✅ Fast-Track Regulatory Approvals – Rwanda offers one of Africa’s fastest trial approval processes (2 months), ensuring rapid study startup. ✅ Globally Recognized Compliance – As one of only 8 African nations with WHO Level 3 certification, Rwanda’s clinical trials meet FDA, EMA, and ICH-GCP standards. ✅ Rapid Patient Recruitment – With a 150,000+ pre-screened patient database, we accelerate enrollment by 50% compared to the U.S. and Europe. ✅ Cost-Efficient Trials – Trials in Rwanda are 50%+ more affordable than in traditional markets. ✅ State-of-the-Art Research Facilities – Trials conducted at Polyclinic du Plateau and the Rwanda Cancer Research Center, ensuring world-class clinical infrastructure. Our Services 🔹 Clinical Trial Execution – Full-service Phase I–IV trials with FDA/EMA compliance. 🔹 Regulatory & Compliance Support – Fast-track approvals, ICH-GCP alignment, and WHO oversight. 🔹 Patient Recruitment & Retention – 150,000+ pre-screened patients, 50% faster enrollment, and 100% retention rates. 🔹 Site Management & Monitoring – Trials at state-of-the-art research centers, with full coordination and compliance oversight. Partner With Nivella Health 📩 Interested in learning more? Contact us today info@nivella.com #ClinicalTrials #Biotech #Pharma #GlobalResearch #CRO #ClinicalResearch #FDACompliance #AfricaClinicalTrials