This is a presentation on improving post-trial access (PTA) arrangements in clinical trials conducted in low- and middle-income countries (LMICs), particularly in Sub-Saharan Africa. The main focus is on establishing ethical, practical, and equitable measures for post-trial access in clinical trials, and creating collaborative frameworks involving stakeholders such as funders, drug regulators, communities, and research ethics committees. This was presented at The Forum for Ethical Review Committees in the Asian and Western Pacific Region Conference 2025 (FERCAP). The full guideline may be accessed here:
zenodo.org