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
Guidelines for Software as Medical Devices
Guidelines for Software as Medical Devices
Guidelines for Medical Device Refurbishment
Guidelines for Medical Device Refurbishment
Guidelines for Medical Device Donations
2022 08 29_Guidelines for Medical Device Donations
Guideline on variation applications to registered vaccines
Guideline on variation applications to registered vaccines
Guidelines for Medical devices Clinical Investigation Authorization
Guidelines for Medical devices Clinical Investigation Authorization
Medical devices Decommissioning and Disposal Guideline
Medical devices Decommissioning and Disposal Guideline
Medical Devices Recall Guideline
Medical Devices Recall Guideline
Guidelines for Medical Devices GMP Inspection
Guidelines for Medical Devices GMP Inspection
Guidelines for Medical device Labeling
Guidelines for Medical device Labeling