EDA Logo
Sorry, this website does not support this browser

Central administration

Central administration Of Pharmaceutical products

General Overview:

  • Evaluation and registration of human and veterinary pharmaceutical preparations, herbal medicines, cosmetics, disinfectants, and household insecticides in accordance with the technical requirements approved by the Authority, ensuring their quality, efficacy, and safety.

  • Assessment and review of stability and bioequivalence studies for locally produced or imported preparations, with the aim of evaluating and approving them. This includes tracking such studies at their execution sites, participating in the licensing of stability centers, conducting periodic reviews of licensed stability centers, and participating in the licensing and periodic review of bioequivalence centers.

Copy Rights @ EDA 2021