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Medicine labels Guidance on TO 91 and TO 92Version 1.1, May 2018Therapeutic Goods AdministrationCopyright Commonwealth of Australia 2018 This work is copyright. You may reproduce the whole or part
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Updated TGA guidance is on the regulations and requirements set forth by the Therapeutic Goods Administration.
Manufacturers, importers, and sponsors of therapeutic goods are required to file updated TGA guidance.
Updated TGA guidance can be filled out online through the TGA portal by providing the necessary information and documentation.
The purpose of updated TGA guidance is to ensure compliance with regulations and safety standards for therapeutic goods.
Information such as product details, manufacturing processes, clinical trials data, and labeling must be reported on updated TGA guidance.
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