EDA - Regulatory Guideline Central Administration of Pharmaceutical Institutions Licensing

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Regulatory Guideline Central Administration of Pharmaceutical Institutions Licensing

النوع	تاريخ الإصدار	الوصف	رقم االأصدار
Guideline	01/2023	Organizational Guideline Regarding the Licensing of Warehouses at the Administration of Medical Products Stores and Warehouses licensing	02
Guideline	12/2023	Regulatory Guidelines of Decree No. 505 of 2021 issued by the Chairman of the Egyptian Drug Authority regarding the licensing requirements for registering companies in the Register of Toll Manufacturers	03
Guideline	01/2024	Organizational Guide for the Procedures of Licensing Scientific Offices	01
Guideline	03/2025	Regulatory Guideline for the Requirements and Procedures of Medical Products Store Licenses and the Health Conditions to be implemented, pursuant to the Decree of the Chairman of the Egyptian Drug Authority No. (725) of 2024	04
Guideline	10/2025	Regulatory Guideline for the Procedures of Operations Licensing of Cosmetics Factories	02
Guideline	10/2025	The Regulatory Guideline for work Procedures of the General Administration of factories licensing	02
Guideline	11/2025	The regulatory guideline for licensing procedures of plasma collection centers and plasma derivatives manufacturing factories, General Administration of Factories Licensing at the Egyptian Drug Authority.	02
Guideline	11/2025	Regulatory Guide for Licensing Requirements of Medical devices Factories, and In vitro diagnostic medical devices	02
Guideline	12/2025	Regulatory Guideline for the Procedures of Registering Managers of Pharmaceutical and Medical Supplies Factories with the General Administration of Factories Licensing	02
Guideline	12/2025	Regulatory Guideline for Certificate Issuance by the General Administration of Certificates and Licensing Follow-up	01
Guideline	03/2026	Technical Requirements for Licensing and Operating – prosthetics, orthotics, And Mobility Aid Factories	02
Guideline	05/2026	Guideline on Procedures For Renewing Technical licenses of Operations for Medical Products and Medical Devices Factories	01
Guideline	06/2026	Regulatory Guideline on the Controls and Procedures for Licensing and Operating Research & Development and Quality Control Laboratories for Medical Products and devices	01
Guideline	07/2026	Guideline of the regulations , requirements and procedures governing the preparation of non-sterile , sterile and hazardous pharmacopeial pharmaceutical products	01
Guideline	07/2026	Guideline on licensing requirements for disinfectants factories / production lines	01

منشورات وكتب دورية

النوع	تاريخ الإصدار	الوصف
قرار رئيس الإدارة المركزية	2010	Decision No. 1 of 2010 regarding procedures for licensing public pharmacies Arabic version
كتاب دوري	2010	Periodic Circular No. 6 of 2010 Arabic version
قرار رئيس الإدارة المركزية	2015	Decision No. 1 of 2015 Arabic version

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