Medical Devices Adverse Event Reporting (MDAER) form
Ethiopian Food and Drug Authority (EFDA) Medical Devices Adverse Event Reporting (MDAER) form for Healthcare professionals and Users MDAER form
Ethiopian Food and Drug Authority (EFDA) Medical Devices Adverse Event Reporting (MDAER) form for Healthcare professionals and Users MDAER form
Guidelines for Medical devices Clinical Investigation Authorization
Medical devices Decommissioning and Disposal Guideline
Medical devices Post Marketing Surveillance Guideline