Please see below for a list of search results.
HTA licensed establishments in the Post Mortem sector are required to report incidents to the HTA - we call these HTARIs - and those in the Human Application and Organ Donation and Transplantation sectors are required to report serious adverse events or...
Congratulations to our Chair, Lynne Berry, who we are delighted to share has been awarded a CBE.
Following on from our announcement earlier this year on the postponement of our inspection activity, we can now confirm that there will be no scheduled site visit inspections this business year.
As a regulator, transparency is not only an aspiration and value, but a statutory duty under the Human Tissue Act. It is also a priority for the Department of Health and Government more generally.
Do I need a licence to import/export starting material for an ATMP from/to the EU?
The Regulations that retain the existing quality and safety standards and provide legal and regulatory certainty after the end of the transition period can be found below: