Guideline for the registration of plasma derived medical products

dc.contributor.author	Ethiopian Food and Drug Authority
dc.date.accessioned	2026-02-24T08:45:33Z
dc.date.available	2026-02-24T08:45:33Z
dc.date.issued	2025
dc.identifier.uri	http://repository.iphce.org/xmlui/handle/123456789/5349
dc.description.abstract	The Ethiopian Food and Drug Authority (EFDA), under Proclamation 1112/2019, regulates all medicinal products, including plasma-derived biological products. Article 30(3) of the proclamation mandates that blood and blood components intended for transfusion or further processing must comply with stringent safety and quality standards before use.	en_US
dc.language.iso	en_US	en_US
dc.subject	Medical supplies	en_US
dc.title	Guideline for the registration of plasma derived medical products	en_US
dc.type	Guideline	en_US