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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 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:
As an establishment, you should risk assess your supply chain of reagents and consumables relating to the handling of tissues and cells.