This page provides a summary of the key pieces of legislation, licensing frameworks, and a brief overview of responsibilities for Designated Individuals (DIs), Named Contacts (ODT sector only), Persons Designated (PDs) and Licence Holders.
Clinicians and transplant teams are responsible for the overall care of donors and recipients, and for assessing the medical suitability of potential donors. The Regulations require the clinician with responsibility for the donor to refer the matter to the HTA. As part of this referral specific information, certain assurances are required to ensure the legislative requirements are addressed.
This section explains the consent exemptions from the Human Tissue Act (2004) (HT Act).
Human bodies, body parts and specimens may be put on public display, for example as part of an exhibition in a gallery or museum. If they are from the body of a deceased person who died less than 100 years ago, the premises must be licensed by the HTA for public display.
Some schools and colleges store human material for use in teaching. Such specimens could include cells on a microscope slide, specimens preserved in formalin, skulls, and partial or complete skeletons.
Under the Human Tissue Act 2004 (‘the HT Act’), human material which contains cells is called ‘relevant material’.