Therapeutic goods act 1989 purpose
WebbThe Therapeutic Goods Act 1989 sets out the legal requirements for the import, export, manufacture and supply of therapeutic goods in Australia; Acts & regulations. … WebbThe Therapeutic Goods Act 1989 Administered by the Therapeutic Goods Administration (TGA) Provides a regulatory framework to ensure therapeutic goods (including medicines) supplied in Australia meet acceptable standards of efficacy, quality and safety.
Therapeutic goods act 1989 purpose
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WebbI. Therapeutic Goods Act 1989 (Cth) regul ation of medicines and medical devices and manufacturers. 1. What the TGA regulates - therapeutic goods including medicines . 1. The T herapeutic G oods A dministration ( TGA ), a part of the Department, regulates therapeutic goods, including medicines, through: x pre- market assessment; http://www5.austlii.edu.au/au/legis/cth/consol_act/tga1989191/s38.html
Webb13 juli 2024 · This is a compilation of the Therapeutic Goods Act 1989 that shows the text of the law as amended and in force on 1 July 2024 (the compilation date). The notes at the end of this compilation (the endnotes) include information about amending laws and the … Therapeutic Goods Act 1989 - C2024C00376; ... Act 2024: An Act … An Act to amend the Therapeutic Goods Act 1989, and for related purposes [Assented … This page lets you browse for the text of legislative instruments. Each main letter … This page lets you browse for the text of notifiable instruments. Each main letter … If you know the title of the Act you want to view, you can enter some or all of the title … This website is managed by the Office of Parliamentary Counsel (OPC) for the … This page lets you browse for the text of Bills and the Explanatory Memorandum. … the text of an amended Act as it is expected to read in the future (only published in … WebbTHERAPEUTIC GOODS ACT 1989 - SECT 41BD. What is a medical device. (1) A medical device is: (a) any instrument, apparatus, appliance, software, implant, reagent, material …
WebbTHERAPEUTIC GOODS ACT 1989 - SECT 31. Secretary may require information or documents. (1) The Secretary may, by notice in writing given to a person: (aa) who is an … Webb17 jan. 2015 · While therapeutic products have many benefits there are risks if they are used inappropriately or not for their intended purpose. Ensuring the benefits of …
WebbTHERAPEUTIC GOODS (MEDICAL DEVICES) REGULATIONS 2002 - made under the Therapeutic Goods Act 1989 TABLE OF PROVISIONS PART 1--PRELIMINARY 1.1.Name of Regulations 1.3.Definitions--the dictionary etc 1.4.Medical devices with a measuring function 1.5.Refurbishment (Act s 3(1)) 1.6.Kinds of medical devices--other common …
http://www5.austlii.edu.au/au/legis/cth/consol_act/tga1989191/s3.html heike simmackhttp://classic.austlii.edu.au/au/legis/cth/consol_act/tga1989191/s41bd.html heike ryu jujitsuhttp://classic.austlii.edu.au/au/legis/cth/consol_reg/tgdr2002400/ heike sinnhttp://classic.austlii.edu.au/au/legis/cth/consol_act/tga1989191/s31.html heike sokollWebb(i) diagnosis, prevention, monitoring, prediction, prognosis, treatment or alleviation of disease; (ii) diagnosis, monitoring, treatment, alleviation of or compensation for an injury or disability; (iii) investigation, replacement or modification of the anatomy or of a physiological or pathological process or state; heikestahn kinesiologieWebbThe Standard for the Uniform Scheduling of Medicines and Poisons ( SUSMP) is an Australian legislative instrument produced by the Therapeutic Goods Administration (TGA). [1] Before 2010, it was known as the Standard for the Uniform Scheduling of Drugs and Poisons ( SUSDP ). [2] heike suekamaWebbTherapeutic goods can comprise a broad range of things, such as bandages, pregnancy testing kits, herbal remedies, tissue grafts and paracetamol. They generally fall under … heike tost