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.

Establishments based in Northern Ireland (NI)

For establishments based in NI a third country is defined as:

  1. in relation to the import of tissues or cells into NI, a country other than NI or an EEA State; and
  2. in relation to the export of tissues or cells from NI, a country other than the UK or an EEA State.

Therefore, if you intend to receive tissues and cells for human application from a supplier based in the EEA, or export tissues and cells for human application to an EEA State or GB, you do not require an import or export licence to do so.

Continuity of supply

Since 1 January 2021, the United Kingdom (UK) has operated a full border with the European Economic Area (EEA). This means that there are changes to the checks and controls on goods (including blood, organs, tissues and cells) as they move between the UK and the EEA.