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Home/Legislation/Therapeutic Goods (Medical Devices) Regulations 2002/Part 8AA

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Therapeutic Goods (Medical Devices) Regulations 2002

Part 8AA—Mandatory reporting of adverse events by healthcare facilities

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## Part 8AA—Mandatory reporting of adverse events by healthcare facilities

Previous section8.1Notice period (Act s 41JA)Next section8AA.1Healthcare facilities

Part Part 8AA - Therapeutic Goods (Medical Devices) Regulations 2002 - —Mandatory reporting of adverse events by healthcare facilities — Zoe