Regulatory & Ethics Support
Running a trial across Sub-Saharan Africa means navigating multiple regulators, ethics committees, and local legal frameworks.
Every African country has its own regulator, its own ethics committee structure, and its own expectations for dossier format, insurance, and import permits. A misread requirement is an extra 60 days on the critical path.
Running a trial across Sub Saharan Africa means navigating multiple regulators, ethics committees, and local legal frameworks. We serve as your local regulatory partner, helping you meet expectations without unnecessary delays.
8
Active
jurisdictions
1st
First-pass
approval
focus
24/7
Safety
reporting
What we do
From first submission to final close-out, fully covered.
Our regulatory footprint
Eight countries. One coordinated submission strategy.
We maintain active relationships with the regulators and ethics committees that govern your trial in each market — and we coordinate timelines so your global program moves as one.
Nigeria
NAFDAC + NHREC
Ghana
FDA + GHS-ERC
Kenya
PPB + KNH-UoN ERC
Uganda
NDA + UNCST
Tanzania
TMDA + NIMR
Rwanda
Rwanda FDA + RNEC
South Africa
SAHPRA + HRECs
Ethiopia
EFDA + NRERC