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The Human Medicines (Amendment) (Modular Manufacture and Point of Care) Regulations 2025
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- UK Statutory Instruments
- 2025 No. 87
- PART 2
- Regulation 29
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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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