46 Reporting requirements
Medicines and Medical Devices Act 2021 (2021 c 3) | Legislation

46  Reporting requirements

(1)     As soon as reasonably practicable after the end of each reporting period, the relevant authority must lay before the appropriate legislature a report on the operation of any regulations made by the relevant authority under sections 2(1), [7A(1),] 10(1), 15(1) and 19(1) that were in force at any time during the reporting period.

(2)     In preparing a report, the relevant authority must consult such

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