16 Manufacture, marketing and supply
Medicines and Medical Devices Act 2021 (2021 c 3) | Legislation

16  Manufacture, marketing and supply

(1)     Regulations under section 15(1) may make provision about—

(a)     requirements that must be met in relation to medical devices in order for them to be marketed, put into service or otherwise supplied (“relevant requirements”), including—

(i)     requirements in terms of design, manufacture, composition or other characteristics of the devices, or

(ii)     requirements imposed on persons involved in marketing or supplying the devices,

(b)     assessments of whether relevant requirements are met in relation to medical devices,

(c)

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