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The HTA was asked to provide information relating to serious adverse events and adverse reactions (SAEARs) in the organ donation and transplantation sector in the year 2015.
The following guidance has been produced to bring clarity to the issues surrounding consent under the Human Tissue Act 2004 for research relating to transplantation where donors are deceased. It applies in England, Wales and Northern Ireland, and is not affected by the Human Transplantation (...
Our Codes of Practice and Standards provide practical guidance to professionals carrying out activities within the scope of the HTA’s remit.
We have created separate documents that provide additional guidance for our licensing Standards for Codes B, C, D and E.
Introduction to the Regulations
The Quality and Safety of Organs Intended for Transplantation Regulations 2012 transpose the European Union Organ Donation Directive (EUODD). The purpose of this Directive is to establish standards for the quality and safety of organs intended for donation...
You can find information about how to meet the requirements of the Regulations in our documentary framework.
Codes of Practice
The HTA has been asked to provide information on how many child bone marrow/blood cases were approved and rejected in the years 2014-15 and 2015-16.