Please see below for a list of search results.
We have been hosting a series of webinars in February and March, to talk about our revised Codes of Practice and Standards, which launch in April.
If you haven't read the updated Codes yet, you can find these on our website here.
Issued 10 May 2017
• Designated Individuals (DIs) in the Human Application (HA) sector
The European Commission is consulting on the EU legislation on blood, tissues and cells.
The guidance will help you to decide whether you need a licence. The guidance will also help you determine which licence you need and the licensable activities it should cover.
Please read this guidance document and prepare your data for submission. It is important that you enter accurate data as you will not be able to make changes once you have submitted the form. We recommend you consider gathering data in advance by sharing this document with your colleagues.
All establishments licensed under the Human Tissue Act 2004 and the Quality and Safety of Organs Intended for Transplantation Regulations 2012 must review their licensing records and complete a compliance update.The information collected will be used to: