Central Administration of Pharmaceutical Products

The Egyptian Drug Authority includes the Central Administration of Pharmaceutical Products, which comprises the following:

• General Administration of Human Product Registration
• General Administration of Cosmetic Products Registration
• General Administration of Herbal Products Registration
• General Administration of Biocides Registration
• General Administration of Veterinary Products
• General Administration of Stability

*Responsibilities of the Central Administration of Pharmaceutical Products:

• Evaluation and registration Human Pharmaceutical Products and Veterinary Pharmaceuticals, Herbal Pharmaceutical Products, Cosmetics, Antiseptics/Disinfectants, and Pesticides in accordance with the necessary technical requirements, approved by EDA, for issuing the market authorization, as well as evaluating and approving variations during the life cycle of those products in order to ensure its quality, efficacy and safety,.
• Assessing and reviewing stability and bioequivalence studies for local & imported pharmaceuticals, for the purpose of evaluating and approving them. And participation in licensing the centers of stability and bioequivalence, and conducting periodic reviews of the licensed centers.