

Subject Matter
On 13 February 2025, the Chairman of the Egyptian Drug Authority (“EDA”) issued Decree No. 39 of 2025 (the “Decree”), which imposes restrictions on the expiry dates and shelf lives of imported pharmaceutical and biological products.
Scope of Application
The Decree applies to all pharmaceutical and biological products imported into Egypt (the “Territory”), including both finished products and those intended for packaging and labelling within the Territory (“Imported Products”).
The Decree will come into effect on 1 July 2025 (the “Effective Date”), repealing any existing regulations or provisions that conflict with its terms.
Key Provisions
Conclusion
The Decree’s subject matter complements the EDA’s recent Decree No. 47 of 2025 on the recall of expired pharmaceutical and biological products, with both aiming to enhance control over the Egyptian pharmaceutical market, ensuring greater stability and reliability.
It is important to note that the anticipated positive impact of such regulations depends on the cooperation of relevant stakeholders to ensure effective enforcement.
The contributors to this article are Fagr Moheb, Managing Associate and Hannah Mahran, Junior Associate.
For further inquiries, please contact our Life Sciences team members Mohamed Abdelgawad, Partner, Head of General Corporate, Commercial, and Regulatory, Fadila Abdelaziz, Counsel, Fagr Moheb, Managing Associate, and Nada Hagag, Associate.