ARO provides integrated clinical research support, strengthened by local expertise
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We assess potential sites based on study requirements, patient population, investigator experience, operational capabilities, infrastructure and regulatory readiness to support informed site selection.
We work with research sites, healthcare providers, and local networks to support the identification and enrollment of eligible participants while keeping patient needs and study requirements at the forefront.
ARO connects sponsors with qualified investigators and research sites across Sub-Saharan Africa, leveraging local relationships and therapeutic-area experience to support study needs.
Compliance is central to how we work. ARO supports navigation of applicable local regulatory and ethics requirements while aligning study activities with ICH-GCP and sponsor requirements.
Our clinical operations and quality teams provide risk-based oversight throughout study execution, supporting site performance, protocol compliance, data quality, and timely identification and management of study risks.
We support clinical trial awareness through engagement with healthcare providers, local clinics and hospitals, patient communities, and other relevant stakeholders to help build understanding and trust around clinical research.
We provide end-to-end support, ensuring trials progress efficiently but with speed.
Site feasibility & recommendations – We evaluate and select ideal research locations.
Principal Investigator engagement – We build relationships with top investigators.
Regulatory approvals & compliance – We ensure trials meet legal and ethical standards.
Site activation & SIV support – We coordinate trial site initiation and investigator training.
Patient recruitment & trial awareness – We execute outreach programs to maximize participation.
Clinical operations & pharmacovigilance – We oversee trial execution, monitoring, and safety.
Laboratory operations & data management – We ensure proper storage, processing, and analysis of trial samples.
IP & clinical supplies management – We handle investigational product logistics and compliance.
Study team training & support – We provide ongoing education for trial staff.
In-country roadshow planning – We establish relationships with key trial sites for long-term partnerships.
ARO provides medical and scientific support tailored to study and regional needs, including medical writing, scientific engagement, investigator support, and other medical affairs activities.
ARO coordinates clinical trial logistics across Sub-Saharan Africa, including importation and customs support, clinical supplies, laboratory logistics, shipment coordination, and last-mile delivery.
ARO develops culturally relevant education and engagement initiatives to strengthen clinical research awareness and understanding among patients, communities, and healthcare providers.
ARO provides practical, on-the-ground support for sponsors, study teams, and partners traveling within Africa, including transportation, accommodation coordination, local navigation, and other in-country logistical needs.
ARO provides local regulatory expertise to help sponsors navigate country-specific regulatory and ethics requirements, including submission planning, regulatory interactions, and guidance throughout the study lifecycle.
ARO supports the planning and coordination of advisory boards and Key Opinion Leader (KOL) engagements, connecting sponsors with relevant clinical, scientific, and healthcare expertise across the region.
Afro-REACH simplifies clinical trials in Sub-Saharan Africa with expert support at every step. Reach out today and let’s get started.
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