Afro-REACH provides expert trial management, site selection, regulatory compliance, and investigator engagement across Sub-Saharan Africa.
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We assess trial sites, select the best locations, and engage Principal Investigators for successful trial execution.
We implement targeted recruitment strategies and awareness programs to ensure patient diversity and enrollment success.
We identify high-potential sites for patient recruitment and successful enrollment.
We streamline submissions and approvals with local regulatory bodies like NAFDAC and NHREC.
We oversee study progress, ensuring data integrity and protocol adherence.
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.
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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