Information about how the HTA and Health Research Authority share infomraion
This section contains guidance about when an HTA licence is required and which application form you need to complete.
Designated Individuals and Licence Holders under the Human Tissue (Quality and Safety for Human Application) Regulations 2007
Here you will find information on Designated Individuals (DIs) and Licence Holders (LHs) under the Human Tissue (Quality and Safety for Human Application) Regulations 2007
EU Directives are being put in place for the coding and import of tissues and cells for human application (HA).
Information about donor decelerations
HTA position statement on storage of human material for teaching by schools and colleges
Public display of body parts
New EU regulations for medical devices (MDR) and in-vitro medical devices (IVDR) have been introduced. These regulations entered into force on 25 May 2017 across EU Member States. However, most requirements will not fully apply until 26 May 2020 for the MDR, and 26 May 2022 for the IVDR.The scope of the MDR now includes certain products manufactured utilising derivatives of tissues or cells of...
Information about reporting a human application or organ donation and transplant SAEAR
Policy on consent for post-mortem examination and tissue retention under the Human Tissue Act 2004