Please see below for a list of search results.
The Transition Period ended on 31 December 2020. This has resulted in regulatory changes within the UK. These may differ for Great Britain and Northern Ireland as the Government ensures it meets its obligation of implementing the Northern Ireland Protocol.
Only authorised users can use the HTA Portal to securely submit their 2020 annual activity data.
EEA: The European Economic Area (EEA) consists of the 28 Member States of the European Union in addition to Iceland, Norway and Liechtenstein.
The table below sets out the tissue types that are reflected in this year’s data collection, and additional guidance on the information we need from you from those tissue types.
Make sure you select ‘save draft’ at regular intervals when inputting your data on the same page. You can save your form at any point so you do not have to do everything in one go.
All establishments licensed to carry out activities under the Human Tissue (Quality and Safety for Human Application) Regulations 2007 must submit data relating to the activities you undertook and the
The framework document contains detailed information on the mandatory regulatory requirements that Organ Donation and Transplantation sector establishments must follow.
The HTA received a request for a list of all of the establishments that held a licence at any time between the 1st of January 2019 and the 31st of December 2019 for the making of a post mortem examination.
The Head of Development works as part of the Regulation Directorate reporting directly to the Director of Data, Technology and Development.
The Policy Manager will both lead on and support colleagues to develop and draft HTA policies on a wide range of issues within the regulatory remit of the organisation. The role will be essential in ensuring the co-ordination of all regulatory development projects.