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Central administration

Central administration Of Pharmaceutical products

General Overview:

  • 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.

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