Boost the performance of your investigation site
Conducting a clinical trial requires rigorous organization, trained teams, and compliant documentation. AFCRA supports investigation sites in Francophone Africa to structure their activities, ensure the safety of their practices, and gain credibility.
Beginner sites
You want to start clinical trials and need structure and support from the outset.
Intermediate sites
You want to improve your performance, your compliance and strengthen your credibility with Sponsors.
Investigators & teams
You wish to establish a sustainable structure and develop expertise in the requirements of clinical research.
Better organization
Complete documentation, guaranteed traceability, standardized processes according to international standards.
Autonomous teams
More competent, more stable and operational teams to conduct clinical studies.
Image reinforced
Increased credibility with Sponsors and CROs, ability to host more studies.
Ready for audits
Reduction of quality gaps and better preparation for audits and inspections by Sponsors.
Is your site ready for international clinical trials?
Let's talk about your situation and define a suitable action plan together.
Contact us