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Under the Human Tissue Act, the HTA has the power to issue its expected standards, or legal Directions, to establishments.

Since 1 January 2021, the United Kingdom (UK) has operated a full border with the European Economic Area (EEA).

The Regulations that retain the existing quality and safety standards and provide legal and regulatory certainty after the end of the UK Transition Period...

The HTA-related licensing changes introduced at the end of the UK Transition Period affect some establishments that previously did not require an HTA licen...

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

Throughout the year we host a programme of stakeholder engagement events.

The duties of the Remuneration Committee are to:

The HTA has a responsibility to make its information available in accordance with the Freedom of Information Act. Before making a Freedom of Informa

You can browse and read previous FOI responses below.