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The Human Medicines (Amendment) (Modular Manufacture and Point of Care) Regulations 2025

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Amendment of regulation 257

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29.  After regulation 257(9) (packaging requirements: general)(1) insert—

(10) Nothing in this regulation applies to a POC medicinal product that is the subject of a UKMA(UK)(Category 1)..

(1)

Regulation 257(9) was inserted by S.I. 2024/832.

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