Adverse event and reaction reporting

This page provides access to the HTA’s system for the reporting of any serious adverse events and/or reactions that are linked to the procurement, testing, processing, preservation, storage and distribution of human tissues and cells.

Please note that if you are not undertaking activities relating to material for human application, for example you carry out post mortems or anatomical examinations, this system is not applicable to you.

If you would like further guidance on whether your establishment can report using the system, please contact Veronica Lindop, Regulation Officer on 020 7211 3438 or email veronica.lindop@hta.gov.uk

Reporting serious adverse events and reactions

Under the European Union Tissue and Cells Directive (EUTCD), the HTA is required to set up a system for tissue establishments to report serious adverse events and reactions. The definitions of serious adverse events and reactions as set out in the EUTCD are as follows:

Serious Adverse Event (SAE)

‘serious adverse event’ means any untoward occurrence associated with the procurement, testing, processing, storage and distribution of tissues and cells that might lead to the transmission of a communicable disease, to death or life-threatening, disabling or incapacitating conditions for patients or which might result in, or prolong, hospitalisation or morbidity.

Serious Adverse Reaction (SAR)

‘serious adverse reaction’ means an unintended response, including a communicable disease, in the donor or in the recipient associated with the procurement or human application of tissues and cells that is fatal, life threatening, disabling, incapacitating or which results in, or prolongs, hospitalisation or morbidity.

Logging in to the notification system

You will need to log in to the system using the same user name and password as when you applied for a licence. Only Designated Individuals (DI) at licensed establishments will currently have a user name and password. Therefore, anyone wishing to use this system who is not reporting from a licensed establishment, will be unable to at present.

Log in to the adverse event and reaction reporting system

The notification system is currently being developed to allow individuals other than the DI to report to the HTA, for example, third party providers and it is hoped that this function will be available in the future. In the meantime, if you are a third party provider or you purchase material from a licensed establishment and you wish to report a serious adverse event or reaction, please contact the DI at the relevant licensed establishment and advise them that they need to report to the HTA on your behalf.  If you would like further guidance on whether your establishment can report using the system, please contact Veronica Lindop, Regulation Officer on 020 7211 3438 or email veronica.lindop@hta.gov.uk 

A requirement of the EUTCD is that you submit notification of a serious adverse event/reaction which is then followed up by the submission of a report once local investigations have taken place. As a user you will have a ‘workspace’ containing a searchable library of all your notifications and follow up reports which only you can access.

Please note that this system does not replace existing local reporting arrangements. In addition to local arrangements you are now required to report to the HTA what you as a professional consider to be a serious adverse event / reaction (not relating to whole organs), as guided by the definitions above. If you are unsure whether to report, please contact Veronica Lindop, Regulation Officer on 020 7211 3438 or email veronica.lindop@hta.gov.uk