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Accredited Assessors submit their reports using the HTA’s online submission system. This is a secure system which is data protected.
It is important that the HTA is able to contact the Designated Individual (DI) and Licence Holder (LH). If your contact details change please let us know. You can email any changes to firstname.lastname@example.org
Read regulatory alert 001/2020
Notice for Designated Individuals in the Human Application sector and licence contacts in the Organ Donation and Transplantation sector regarding West Nile Virus.
The Human Fertilisation and Embryology Authority (HFEA) and the Human Tissue Authority (HTA) have been working together to reduce the regulatory overlap regarding the storage of ovarian and testicular tissue.
It is a mandatory requirement that the processes used to prepare tissue or cells for patient treatment (human application) do not render them clinically ineffective or harmful, and they must be validated.
The validation of the processes may be based on:
The McCracken review looked at how the HTA and HFEA could be more efficient. The HTA has fully incorporated its recommendations.
In order to increase the accessibility of this site, we have provided a number of Access keys. These are keyboard shortcuts providing an alternative form of navigation.
The Human Tissue Authority (HTA) is the national independent regulator for organisations that remove, store and use tissue for research, medical treatment, post-mortem examination, teaching and display in public. We also give approval for organ and bone marrow donations from living people.
Accuracy of informationPlease note the following: Every effort has been made to ensure that the information provided on this website is accurate, but accuracy cannot be guaranteed and the information provided does not constitute legal or other professional advice.