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Announcements 09/11/MDS-AN010  NEW

Important notice regarding Supply of Medical Devices to Saudi Arabia

Announcements 05/11/MDS-AN009  Updated

Update of the Implementing Rule on LICENSING OF AUTHORISED REPRESENTATIVES (MDS-IR5) and the Guidance for Medical Device Authorised Representatives (MDS – G3).

Announcements 12/10/MDS-AN001

( Update of the Implementing Rule on the Validation of Documents to be provided to the SFDA by Manufacturers for Marketing Authorization (MDS-IR6) and in particular its application dates.

Announcements 12/10/MDS-AN002

( Publication of Guidance documents in relation to the Medical Devices Interim Regulation and its Implementing Rules.

Announcements 12/10/MDS-AN003

( Publication of Marketing Authorization application fees and review times.

Announcements 12/10/MDS-AN005

( Publication of Authorized Representative application fees and review times.

Announcements 12/10/MDS-AN006

( Publication of Establishment licensing application fees and review times.

Announcements 02/11/MDS-AN007

(Launching of Medical Device Marketing Authorization (MDMA) system.

Announcements 02/11/MDS-AN008

(Launching the new version of Medical Device Establishment Licensing (MDEL) system.