We simplify the complexities of Nigeria’s regulatory environment, ensuring smooth and compliant study approvals.
Managing national and institutional ethical approvals.
Handling IND and Clinical Trial Authorization (CTA) applications.
Managing national and institutional ethical approvals.Facilitating compliant entry of investigational products and clinical supplies.
Data-driven insights to set your study up for success from day one.
Evaluating disease prevalence across Nigeria’s regions.
Assessing infrastructure, equipment, and staff readiness.
Delivering realistic enrollment projections based on hospital data.
Maintaining the highest standards of data integrity and patient safety.
Training site teams on protocol and study requirements.
On-site and remote oversight to ensure ICH-GCP compliance.
Validating accuracy and reliability of trial data.
Serving as the critical link between sponsors and clinical sites.
Ongoing GCP and protocol-specific training.
Dedicated coordinators to streamline site operations.
Access to a trusted network of hospitals and clinics across Nigeria.