dc.contributor.author | Ethiopian Food and Drug Authority | |
dc.date.accessioned | 2023-12-27T06:23:33Z | |
dc.date.available | 2023-12-27T06:23:33Z | |
dc.date.issued | 2023-05 | |
dc.identifier.uri | http://repository.iphce.org/xmlui/handle/123456789/2656 | |
dc.description.abstract | Medical products cannot be treated in the same way as ordinary commodities. Their manufacture and subsequent handling within the distribution chain must conform to prescribed standards and be rigorously controlled. These precautions serve to assure that patients receive quality assured medical products, and to prevent the infiltration of substandard and suspected falsified medical products into the supply system | en_US |
dc.language.iso | English | en_US |
dc.subject | Medical supplies | en_US |
dc.title | Guideline on medical products special import permit | en_US |
dc.type | Guideline | en_US |