[7A Information systems]
Medicines and Medical Devices Act 2021 (2021 c 3) | Legislation

[Chapter 1A
Regulations: Information Systems]

[7A  Information systems]

[(1)     The appropriate authority may by regulations make provision about the establishment and operation by [NHS England] of one or more information systems for purposes relating to—

(a)     the safety of human medicines, including the safety of clinical decisions relating to human medicines;

(b)     the quality and efficacy of human medicines.

(2)     The regulations may (among other things) make provision—

(a)     about the information in relation to human medicines which may or must be entered or retained in an information system established under subsection (1);

(b)     requiring information to be provided to [NHS England] for the purposes of its functions under the regulations;

(c)     about the use or disclosure of information contained in an information system established under subsection (1);

(d)     requiring [NHS England] to have regard to specified matters in exercising its functions under the regulations.

(3)     The provision mentioned in subsection (2)(a) and (b) may relate to—

(a)     information for specified purposes,

(b)     information that [NHS England] considers it necessary or expedient to have for the purposes of its functions under the regulations,

(c)     information (including information relating to individuals) which is of a specified description, or

(d)     information (including

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