The Egyptian Drug Authority (EDA)—represented by the Central Administration for Medical Devices—announces a public consultation regarding the fourth edition of the regulatory guideline for procedures and rules regulating amendments to registration notification data of imported medical devices holding international quality certificates. We are honored to receive any comments or proposals through the dedicated feedback form, the Stakeholder Feedback Form, via email at: md.variation@edaegypt.gov.eg

This will be effective starting today, Monday, 19/10/2026, for a duration of 10 working days.

To view the regulatory guideline, please click on the link.