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Importing tissue establishments must ensure that imports from third countries meet standards of quality and safety equivalent to those in the UK.

New EU regulations for medical devices (MDR) and in-vitro medical devices (IVDR) have been introduced.

As a regulator, transparency is not only an aspiration and value, but a statutory duty under the Human Tissue Act.

The HTA licenses establishments in the anatomy sector to provide assurance to the public that bodies or tissue from the deceased are given with proper cons...

Medical school staff are sometimes faced with the challenge of deciding whether the consent given by potential donors, often many years before their death,...

Guidance on how establishments can improve their body donation information.

This section explains the consent exemptions from the Human Tissue Act (2004) (HT Act).

Disposal of relevant material is one of the statutory activities within the remit of the Human Tissue Authority (HTA).

This page contains information on changing, updating or closing your HTA licence including changes to the Designated Individual (DI), Li

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