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This paper looks at why New Zealand first created, and then quickly repealed, a new law (the Therapeutic Products Act 2023) that would have updated how medicines, medical devices and natural health products are regulated. The Act would have checked device safety before products reached the market (“pre-market approval”) and covered health software (“software as a medical device”, meaning apps or programs used for diagnosis or care), but those features did not carry over after repeal. It also formally acknowledged Rongoā Māori (traditional Māori healing), whereas the repeal-era papers did not address Rongoā or Te Tiriti considerations. The analysis compares official documents and submissions to show how the policy narrative switched from safety and modernisation to cutting “red tape” and what protections were lost as a result.