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The HTA regulates establishments in England, Wales and Northern Ireland that conduct licensed activities under the Human Tissue Act 2004 (HT Act).

Procurement is defined as the processes by which tissues and cells are made available, including the physical act of removing tissue and the donor selectio...

In 2010, the HTA developed a new licence fee structure which has been in operation since 1 April 2011.

The HTA licenses and inspects organisations across the six different sectors.

Human bodies, body parts and specimens may be put on public display, for example as part of an exhibition in a gallery or museum.

The purpose of this guidance is to set out our policy on human tissue xenografts, whether they are relevant material that fall under the licensing framewor...

The definition of relevant material in the Act is: Section 53: Relevant material:

Guidance for professionals in licenced mortuaries on reporting incidents. (HTARIs).

Under the Human Tissue (Quality and Safety for Human Application) Regulations 2007 (Q&S Regulations), the HTA licenses and inspects establishments that...

This guide explains the regulatory requirements for establishments in the Human Application sector.

It is a mandatory requirement that the processes used to prepare tissue or cells for patient treatment (human application) do not render them clinically in...

The list below provides guidance on which types of tissues and cells are regulated under the Human Tissue (Quality and Safety for Human Application) Regu

The Designated Individual (DI) at the licensed establishment is responsible for ensuring suitable practices take place under the authority of the Human Tis...

Issued 17 August 2009