EDE FederalFederal Decree-Law No. 38 of 2024
Federal Decree-Law No. 38 of 2024 is the official EDE identifier for “Federal Decree-Law Governing Medical Products, Pharmacists and Pharmaceutical Establishments”. Federal Decree-Law No. 38 of 2024 is the official identifier EDE uses for this instrument.
- Instrument
- Federal
- Full name
- Federal Decree-Law No. 38 of 2024
- Category
- General
- Authority source
- English
- Readable HTML
- 181 articles · 1 language version
- Published
- 2024-10-14
- Effective
- 2025-01-02
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Each version has stable passage anchors for direct citations and highlighting. The readable text is generated from an authority source and does not replace the legally controlling publication.
Federal Decree-Law Governing Medical Products, Pharmacists and Pharmaceutical Establishments
Primary law for medical products, including Medical Equipment, in force from 2 January 2025. It assigns marketing approval and oversight functions to EDE alongside responsibilities of the Ministry and competent health authorities, and repeals Federal Law No. 8 of 2019 subject to the transition in Article 180. The complete official English expression includes the preamble, nine Parts, twelve Chapters and 181 articles. The Arabic original prevails in interpretation and application.
Federal Decree-Law No. 38 of 2024 is the official identifier EDE uses for this instrument. Always confirm the current consolidated text and transition provisions with the official source before filing.