SFDA, Good Manufacturing Practice for Blood Establishments.

SFDA (Saudi Food & Drug Authority) adopted on 06 June 2018 , Good Manufacturing Practice for Blood Establishments. The purpose of this document is to provide guidance for GMP-inspectors and useful information for blood establishments relating to the collection, preparation, storage, dispatch, quality control and quality assurance of blood and blood components. For more information here is the Link to the complete document: https://www.sfda.gov.sa/en/drug/drug_reg/Regulations/DrugGMPBloodEstablishments.pdf