The report is the result of the joint efforts of and collaboration between healthcare professionals and the Commission. It summarises Serious Adverse Reactions and Events (SARE) data for 2021 submitted by 26 Member States plus...
The report summarises Serious Adverse Reactions Events (SARE) data for the year 2021 submitted to the Commission by 30 European countries and includes major findings, general conclusions and trends in European transfusion services in terms...
The report, prepared by the European Directorate for the Quality of Medicines & HealthCare, summarises Serious Adverse Reactions and Events (SARE) data for the year 2020 (submitted to the Commission by 30 European countries), elaborates...
The report summarises the data submitted by the Member States, Norway and the United Kingdom during 2021, collected by the reporting countries during 2020, highlights major findings, draws general conclusions, and interprets trends by comparing...
Publication of the 2022 annual report of the Vigilance Expert Subgroup of the National Competent Authorities for Substances of Human Origin Expert Group. Read the news published by EC Directorate-General for Health and Food Safety...
HTA licensed establishments in the Post-Mortem, Human Application and Organ Donation and Transplantation sector are required to report incidents to the HTA as part of their licensing requirements. In the post-mortem sector these are called...
The Competent Authorities on Substances of Human Origin (CASoHO) Expert Group agreed with the Commission’s services in 2017 to establish an Expert Sub-Group on Vigilance of Blood, Tissues and Cells, referred to as the ‘VES’....
For more info on dates, formats and registration, please follow the link.
