Ethiopia
The new article covers the matters related to the preparation of the reports, GMP quality assurance, administrative measures, and complaint handling procedures. Table of Contents The Ethiopian Food and Drug Administration (EFDA), the...
Ethiopia
The new article addresses the matters related to the technical competence and training requirements for inspectors, as well as to their responsibilities. Table of Contents The Ethiopian Food and Drug Authority (EFDA), a country’s...
Ethiopia
The article provides a brief overview of the Ethiopian guidelines for medical device manufacturers’ Good Manufacturing Practices site inspection management. Table of Contents The Ethiopian Food and Drug Administration (EFDA), a country’s...
Ethiopia
The new article provides additional details regarding the regulatory requirements to be applied concerning labeling for certain types of medical devices, including the in vitro diagnostic (IVD) and sterile products, as well as active and implantable medical devices. ...
Ethiopia
The new article describes in detail certain specific aspects related to the labeling for medical devices intended to be marketed and used in Ethiopia, including the way the labeling should be placed and the information it should contain. ...
Ethiopia
The article provides an overview of the regulatory requirements for medical device labeling introduced in Ethiopia. Table of Contents The Ethiopian Food and Drug Authority (EFDA), a country’s regulatory agency in the sphere of healthcare...
