Medical Devices

Guidance on Requirements for Reporting of Incident and Adverse Event of Medical Devices

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Saudi Food and Drug Authority

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Announcement (8) 8/2019 (Replacement for ANNOUNCEMENT 01/14 MDS-AN015)

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Guidance on Requirements for Unique Device Identification (UDI) for Medical Devices

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Announcement ( 6 ) 5/2019

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MD Registration Draft

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GUIDANCE FOR MEDICAL DEVICE IMPORTERS AND DISTRIBUTORS

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GUIDANCE FOR LOCAL MANUFACTURERS

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GUIDANCE FOR MEDICAL DEVICE AUTHORIZED REPRESENTATIVES

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GUIDANCE FOR OVERSEAS MANUFACTURERS

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GUIDANCE ON MARKETING AUTHORIZATION PROCEDURES

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GUIDANCE ON POST-MARKETING SURVEILLANCE

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Guidance on Medical Devices Bundling/ Grouping Criteria

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GUIDANCE ON MEDICAL DEVICES INTENDED FOR DEMONSTRATION OR TRAINING PURPOSES ONLY

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GUIDANCE ON INTERNATIONAL QUALITY AND EFFICIENCY SAMPLES

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GUIDANCE ON MEDICAL DEVICES ADVERTISING REQUIREMENTS

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