I am Begumisa Casmil, I hold a 4 years bachelor of pharmacy degree with Honours and possess seven (7) years of experience in regulatory affairs to include the technical knowledge of the medicine’s regulatory environment of which, two years is in the hospital setting as Hospital Pharmacist. Currently, my basic responsibilities as Drug Registration Officer at Tanzania Medicines and Medical Devices Authority (TMDA) are to review and evaluate documentation of products (human, veterinary medicines, vaccines and including biological products) applied for registration for marketing authorization by ensuring quality, safety and efficacous of medicinal product are in place in order to improve, protect and promote public health.

Also, I am Focal Person for coordination of the implementation of the Memorandum of Understanding (MoU) on cooperation in the regulation of medical products between the Government of the United Republic of Tanzania and other National Regulatory Authorities (NRAs) . Whereas I coordinate all matters related to regulatory activities including Marketing Authorization, GMP, GCP, PMS, WHO Maturity Level, sharing of information, training and attainment of mutual recognition status level.