You are here Home Resources and guidance Guidance Supplying therapeutic goods that contain human blood or plasma Guidance on the regulatory requirements for therapeutic goods that contain, or are produced from, human blood or plasma. Published 9 August 2013 Last updated 9 August 2013 Listen Print Share LinkedIn (Twitter) Facebook Email Save as PDF Loading... Recently published This page was published on [date_placeholder]. Recently updated This page was updated on [date_placeholder]. See page history for details. This webpage is under review. Please contact bloodandtissues@health.gov.au for further information. Legislation Therapeutic Goods Act 1989 Product types Human cell and tissue products Featured in Prescription medicines collection Page history