Updated 13 April 2012
Tissue establishments handling human tissues and cells in connection with the testing, processing, preservation, storage, distribution, import or export for human applications must hold an authorisation issued by the Danish Health and Medicines Authority.
Section 16(2) of the Danish Tissue Act provides that the Danish Medicines Agency (now the Danish Health and Medicines Authority) must keep a register of these Danish tissue establishments and other public or private organisations.
The list of authorised tissue establishments is now available at the website of the Danish Health and Medicines Authority (in Danish only). See the link to the right.