Human Tissue Authority

The regulator for human tissue and organs

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    Clarification of the scope of the Medical Devices Regulation for tissues and cells products
    Date published: November 2017

    New EU regulations for medical devices (MDR) and in-vitro medical devices (IVDR) have been introduced. These regulations entered into force on 25 May 2017 across EU Member States. However, most requirements will not fully apply until 26 May 2020 for the MDR, and 26 May 2022 for the IVDR.
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    Clarification of the scope of the Medical Devices Regulation for tissues and cells products
    Date published: November 2017

    New EU regulations for medical devices (MDR) and in-vitro medical devices (IVDR) have been introduced. These regulations entered into force on 25 May 2017 across EU Member States. However, most requirements will not fully apply until 26 May 2020 for the MDR, and 26 May 2022 for the IVDR.
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    HTA responds to Government's regenerative medicine report
    Date published: March 2015

    The Human Tissue Authority (HTA) welcomes the publication of the report from the Regenerative Medicine Expert Group, “Building on our own potential: a UK pathway for regenerative medicine”.
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    HTA’s Correspondence with University of Bristol regarding a trachea transplant in 2008
    Date published: October 2016

    The HTA was asked to share a letter written to the University of Bristol regarding a process taking place at the university in 2008, as part of a process to create an artificial trachea for transplant
    HTA’s Correspondence with University of Bristol regarding a trachea transplant in 2008