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Cover of the report "Survey on testing strategies for HIV in blood, tissues and cell donors within the EU/EEA"

Assessment

Survey on testing strategies for HIV in blood, tissues and cell donors within the EU/EEA

09 April 2025
Report on the findings of a survey on testing strategies for HIV in blood, tissues and cell donors within the EU/EEA at the time of development of ECDC guidelines for the prevention of donor-derived transmission of human immunodeficiency virus (HIV) through SoHO.
Survey on testing strategies for HIV in blood, tissues and cell donors within the EU/EEA - EN - [PDF-2.33 MB]

Surveillance and monitoring

Risk of transmission of Ebola virus via donated blood and other substances of human origin in the EU

06 October 2014
This technical report assesses the risk of Ebola virus transmission through substances of human origin and offers guidelines on the safety of donations where the potential donors are travellers returning from Ebola-affected countries, people exposed to Ebola virus or patients who have recovered from the disease.
Risk of transmission of Ebola virus via donated blood and other substances of human origin in the EU - EN - [PDF-68.15 KB]
Thumbnail

Surveillance and monitoring

Laboratory testing of non-partner sperm donors

20 June 2018
The European Centre for Disease Prevention and Control was asked by the European Commission to assess the risk involved in changing the testing requirements for HIV (human immunodeficiency virus), hepatitis B virus (HBV), and hepatitis C virus (HCV) with regard to the quality and safety of non-partner semen donations.
Laboratory testing of non-partner sperm donors - EN - [PDF-1.5 MB]

Risk assessment

Risk assessment of HTLV-I/II transmission by tissue/cell transplantation

03 April 2012
Following a request from the European Commission in August 2010, ECDC assessed the epidemiological history of Human T-lymphotropic Virus (HTLV) across the world, possible risks of HTLV transmission through transplantation of human tissues and cells, and possible measures to prevent such transmission.
120403-RA-Human-T-lymphotropic-Virus-transmission.pdf - EN - [PDF-840.41 KB]
Thumbnail

Risk assessment

Risk assessment: The risk of variant Creutzfeldt-Jakob disease transmission via blood and plasma-derived medicinal products manufactured from donations obtained in the United Kingdom

03 August 2021
ECDC assessed the risk to the EU/EEA of the presence and the possible transmission of prions, which have been linked to Creutzfeldt-Jakob disease, by blood and plasma-derived medicinal products (PDMPs) manufactured from donations obtained in the UK.
The risk of variant Creutzfeldt-Jakob disease transmission via blood and plasma-derived medicinal products manufactured from donations obtained in the United Kingdom - EN - [PDF-713.64 KB]
Thumbnail

Public health guidance

Coronavirus disease 2019 (COVID-19) and supply of substances of human origin in the EU/EEA - Third update

23 August 2023
This document provides an update on the safety of substances of human origin (SoHO) in relation to COVID-19. It reassesses the risk and proposes revised mitigation measures for preventing transmission through SoHO.
Coronavirus disease 2019 (COVID-19) and supply of substances of human origin in the EU/EEA - Third update - EN - [PDF-484.98 KB]

Risk assessment

Questions on variant Creutzfeldt–Jakob disease and blood transfusion

01 July 2011
Two developments in the field of variant Creutzfeldt–Jakob disease (vCJD) occurred in 2009. In order to address a number of questions that were raised, ECDC internal and external experts prepared this risk assessment. The document focuses on how these new facts affect the current assumptions regarding transmissibility of the disease through blood transfusion and tissue/cells transplantation.
110921_TER_Risk assessment_vCJD.pdf - EN - [PDF-598.7 KB]
Suspected adverse reactions to COVID-19 vaccination and the safety of substances of human origin

Surveillance and monitoring

Suspected adverse reactions to COVID-19 vaccination and the safety of substances of human origin

03 June 2021
The purpose of this document is to address the safety of donors and products involving Substances of Human Origin (SoHO) and the potential risk of thrombosis with thrombocytopenia adverse events following COVID-19 vaccination of a donor.
Suspected adverse reactions to COVID-19 vaccination and the safety of substances of human origin - EN - [PDF-558.79 KB]

Risk assessment

Risk assessment of HTLV-I/II transmission by tissue/cell transplantation – Part 2: Risks by tissue type, impact of processing and effectiveness of prevention measures

20 June 2012
Following a request from the European Commission in August 2010, ECDC assessed the epidemiological history of Human T-lymphotropic Virus (HTLV) across the world, possible risks of HTLV transmission through transplantation of human tissues and cells, and possible measures to prevent such transmission.
20120620_RA_HTLV_Part2.pdf - EN - [PDF-781.02 KB]

Risk assessment

Risk assessment on change of testing requirements for partner donation of reproductive cells

12 June 2012
In May 2011, the European Commission asked ECDC to estimate the change in total exposure risk to hepatitis B (HBV), hepatitis C (HCV) and human immunodeficiency virus (HIV) during reproductive cell handling and storage for secondary parties, if the current scheme of testing at each cell donation would change to testing partner donors of reproductive cells once or twice a year.
1206-RA-donation-reproductive-cells.pdf - EN - [PDF-1.74 MB]

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