About me
Dr. Motiur Rahman is a Senior Epidemiologist and Policy Advisor in Real-World Evidence (RWE) Analytics within the Office of Medical Policy at CDER, FDA. He leads the consult service for reviewing RWD study submissions, leads international regulatory collaborations including ICH initiatives, and supports internal training and process development. He serves as FDA topic lead for the ICH E23 Working Group, contributes to FDA-funded demonstration projects, and is a core member of the RWE Subcommittee. Dr. Rahman joined FDA in 2022 after more than a decade of academic and industry experience conducting observational studies across diverse therapeutic areas.
