Guidance on Requirements for Reporting of Incident and Adverse Event of Medical Devices + Saudi Food and Drug Authority + Announcement (8) 8/2019 (Replacement for ANNOUNCEMENT 01/14 MDS-AN015) + Guidance on Requirements for Unique Device Identification (UDI) for Medical Devices + Announcement ( 6 ) 5/2019 + MD Registration Draft + GUIDANCE FOR MEDICAL DEVICE IMPORTERS AND DISTRIBUTORS + GUIDANCE FOR LOCAL MANUFACTURERS + GUIDANCE FOR MEDICAL DEVICE AUTHORIZED REPRESENTATIVES + GUIDANCE FOR OVERSEAS MANUFACTURERS + GUIDANCE ON MARKETING AUTHORIZATION PROCEDURES + GUIDANCE ON POST-MARKETING SURVEILLANCE + Guidance on Medical Devices Bundling/ Grouping Criteria + GUIDANCE ON MEDICAL DEVICES INTENDED FOR DEMONSTRATION OR TRAINING PURPOSES ONLY + GUIDANCE ON INTERNATIONAL QUALITY AND EFFICIENCY SAMPLES + GUIDANCE ON MEDICAL DEVICES ADVERTISING REQUIREMENTS +
