Dr. Rifat Ara (Bangladesh) described the evolution of Bangladesh’s cancer registries, which remain primarily hospital-based since 2005, with no nationwide population registry. Data collection is mostly paper-based, with limited electronic tracking through screening programs for cervical and breast cancer. Challenges include lack of awareness, unequal access to care, inadequate reporting (especially from private facilities), and resource constraints. Barriers specific to cervical cancer registration involve cultural stigma, weak referral systems, and fragmented databases. Plans include digitization, making cancer a notifiable disease, equitable care expansion, and establishing eight regional comprehensive cancer centers to serve as registry hubs.