Official version of legislation
The Federal Register of Legislation is the authorised Australian Government website for Commonwealth legislation. It contains the full text and details of the life cycle of individual laws.
Guidance referring to this legislation
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GuidanceThis guidance explains how sponsors should prepare, submit and maintain a Type I Plasma Master File (PMF) for therapeutic goods for supply in Australia that contain or are produced from human blood or plasma.
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GuidanceGuidance on when a manufacturing licence is required for manufacturing medicinal maggots and how a time-limited Goods Manufacturing Practice (GMP) exemption applies. Understand your regulatory obligations when producing medicinal maggot products in Australia.
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