OPTIMIZING CLINICAL MONITORING IN AFRICA
Clinical monitoring for research in Africa can be challenging.
Clinical monitoring in Africa can be difficult because of varying clinical site practices (SOPs), ICH-GCP experience, and regulatory guidelines.
While global CROs provide a sense of familiarity, they lack agility and adaptability unique to clinical research in Africa. Their cumbersome data collection and oversight approach don’t just strain budgets—they stretch timelines and overwhelm sites, leading to diminished enthusiasm.
EXPERIENCED CLINICAL RESEARCH ASSOCIATES (CRAs)
CRAs with 5+ years of experience in clinical monitoring in Africa, therapeutic expertise, and regional knowledge and experience for efficient trial management.
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Make a difference in patients’ lives by setting your clinical trial on the path to success today.