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The Factory Licensing Department for Medical Supplies and Laboratory Diagnostics is a subdivision of the General Administration for Factory Licensing under the Central Administration for Operations.
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The Medical Devices and Laboratory Diagnostics Inspection Department is a division under the General Administration for Factory Inspection, part of the Central Administration for Operations.
It is responsible for inspecting factories of medical supplies, medical devices, laboratory diagnostics, and companies importing medical supplies and laboratory diagnostics.
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This department is part of the Central Administration for Medical Devices, responsible for evaluating and registering locally produced or imported medical Devices and issuing registration notifications after verifying compliance with the required technical standards approved by the authority
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The Department for Laboratory Diagnostics and Device Registration is a division under the General Administration for Market Authorization, which is part of the Central Administration for Medical Devices. It handles issuing import approvals for diagnostics and laboratory devices.
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This department is part of the Central Administration for Pharmaceutical Control, tasked with ensuring the quality and regulation of medical devices and diagnostics locally and internationally.
The Reference Laboratory is one of the divisions of the Research and Development Center, providing regulatory services to manufacturers of medical devices and pharmaceutical products.
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The Export Support and Monitoring Department is part of the General Administration for Export Support and Investment Promotion under the Central Administration for Pharmaceutical Policies and Market Support. It is responsible for issuing all types of export approvals
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