Disclosing information on incidents

HTA licensed establishments in the Post-mortem sector are required to report incidents to the HTA - we call these HTARIs - and those in the Human Application and Organ Donation and Transplantation sectors are required to report serious adverse events or reactions (SAEARs), as part of their licensing requirements.

In line with the HTA's commitment to transparency, we will be publishing reports every quarter detailing the volume and nature of incidents reported. 

 

Freedom of Information

The HTA has a responsibility to make its information available in accordance with the Freedom of Information Act. Before making a Freedom of Information request please take the time to check that it is not already available on one of these pages:

Authority Board

The Authority – the HTA’s non-executive board – is made up of a Chair and 11 Members who are appointed by the Secretary of State for Health, with the exception of one Member appointed by the Welsh Minister and one by the Minister in Northern Ireland.

Existing HTA licence holders

The six-month phase for Human Application sector establishments to comply with new import and export licensing requirements ended on 1 July 2021.

If you import or export tissues and cells between GB and the EEA, you may need a suitable HTA licence in place covering this activity. If you think this applies to you and you have not previously contacted us to discuss your arrangements, please contact us as soon as possible.