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Schedule 1 of the Human Tissue Act 2004 (the Act) sets out ‘performance assessment’ as a ‘scheduled purpose’.
An HTA licence is required if the human cellular material (‘relevant material’) to be stored for performance assessment has been removed from the deceased.
Our Codes of Practice and Standards provide practical guidance to professionals carrying out activities within the scope of the HTA’s remit.
We have created separate documents that provide additional guidance for our licensing Standards for Codes B, C, D and E.
Role of Designated Individual
Designated Individuals have a key role to play in implementing the requirements of the HT Act.
Our Codes of Practice and Standards provide practical guidance to professionals carrying out activities within the scope of the HTA’s remit.
This position statement outlines guidance provided on consent for post-mortem examination and tissue retention.
The GMC provides guidance setting out good practice principles for doctors involved in research.
Under the Human Tissue Act 2004, the HTA is required to license the storage of relevant material for ‘research in connection with disorders, or the functioning, of the human body’.