SFDA - Medical Device Marketing Authorisation System

Use your MDNR User Name and Password to login Only for Local Manufacturer Authorised Representative. As a result the SFDA launched a comprehensive marketing authorisation program intended to safeguard public health as it relates to medical devices. The program comprises two major steps. Establish an overall profile of the medical devices presently on the Kingdom of Saudi Arabia KSA market. In fulfillment of Medical Devices Interim Regulation chapter Two and chapter Six in addition to Implementing.

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الإدارة التنفيذية للرقابة على الغذاء المستورد. الإدارة التنفيذية للوائح الفنية والمواصفات. الإدارة التنفيذية للرقابة على الأسواق المحلية. الإدارة التنفيذية لمراكز الرصد وإدارة الازمات. قائمة الأدوية والمستحضرات العشبية المسجلة. قائمة الصيدليات المرخص لها ببيع الادوية النفسية. الاسئلة الشائعة لنظام الباركود ثنائي الابعاد. لائحة رقابة الأجهزة والمنتجات الطبية. 2013, جميع الحقوق مح.

الهيئة العامة للغذاء والدواء

الإدارة التنفيذية للرقابة على الغذاء المستورد. الإدارة التنفيذية للوائح الفنية والمواصفات. الإدارة التنفيذية للرقابة على الأسواق المحلية. الإدارة التنفيذية لمراكز الرصد وإدارة الازمات. قائمة الأدوية والمستحضرات العشبية المسجلة. قائمة الصيدليات المرخص لها ببيع الادوية النفسية. الاسئلة الشائعة لنظام الباركود ثنائي الابعاد. لائحة رقابة الأجهزة والمنتجات الطبية.

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SFDA - Medical Device Marketing Authorisation System

DESCRIPTION

Use your MDNR User Name and Password to login Only for Local Manufacturer Authorised Representative. As a result the SFDA launched a comprehensive marketing authorisation program intended to safeguard public health as it relates to medical devices. The program comprises two major steps. Establish an overall profile of the medical devices presently on the Kingdom of Saudi Arabia KSA market. In fulfillment of Medical Devices Interim Regulation chapter Two and chapter Six in addition to Implementing.

PARSED CONTENT

The website mdma.sfda.gov.sa states the following, "Use your MDNR User Name and Password to login Only for Local Manufacturer Authorised Representative." I viewed that the webpage said " As a result the SFDA launched a comprehensive marketing authorisation program intended to safeguard public health as it relates to medical devices." They also said " The program comprises two major steps. Establish an overall profile of the medical devices presently on the Kingdom of Saudi Arabia KSA market. In fulfillment of Medical Devices Interim Regulation chapter Two and chapter Six in addition to Implementing."

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