Regulation 15 Equipment: general duties of the employerI1
England, Wales and Scotland
An employer who has control over any equipment must—
implement and maintain a quality assurance programme in respect of that equipment which must as a minimum permit—
the assessment of the dose of ionising radiation that a person may be exposed to from an exposure to which these Regulations apply, by way of the ordinary operation of that equipment; and
the administered activity to be verified;
draw up, keep up-to-date and preserve at each radiological installation an inventory of equipment at that installation and, when so requested, must provide it to the relevant enforcing authority.
The inventory referred to in paragraph (1)(b) must contain the following information F1for equipment other than software—
name of manufacturer;
model number;
serial number or other unique identifier;
year of manufacture; and
year of installation.
The inventory referred to in paragraph (1)(b) must contain the following information for equipment that is software—
name of software company;
brand name;
current software version;
year of original installation; and
year of current software version installation in clinical use.
An employer must undertake adequate—
testing of any equipment before it is first used for F3an exposure to which these Regulations apply;
performance testing at regular intervals;
performance testing following a maintenance procedure which is capable of affecting the equipment’s performance.
A person must not use fluoroscopy equipment unless that equipment features—
a device to control automatically the dose rate; or
an image intensifier or equivalent device.
Equipment used for interventional radiology and computed tomography must have a device or other feature capable of informing the F4operator, at the end of an exposure of relevant parameters for assessing the patient dose.
An employer must—
put in place any measures necessary to improve inadequate or defective performance of equipment;
specify acceptable performance criteria for equipment; and
specify what corrective action is necessary when, following the application of any criteria specified under paragraph (b), equipment is ascertained to be defective; such corrective action may include taking the equipment out of service.
Annotations
Textual amendments
- F1
Words in reg. 15(2) inserted (1.10.2024) by The Ionising Radiation (Medical Exposure) (Amendment) Regulations 2024 (S.I. 2024/896), regs. 1(2), 14(2)
- F2
Reg. 15(2A) inserted (1.10.2024) by The Ionising Radiation (Medical Exposure) (Amendment) Regulations 2024 (S.I. 2024/896), regs. 1(2), 14(3)
- F3
Words in reg. 15(3)(a) substituted (1.10.2024) by The Ionising Radiation (Medical Exposure) (Amendment) Regulations 2024 (S.I. 2024/896), regs. 1(2), 14(4)
- F4
Word in reg. 15(5) substituted (1.10.2024) by The Ionising Radiation (Medical Exposure) (Amendment) Regulations 2024 (S.I. 2024/896), regs. 1(2), 14(5)
Commencement
- I1
Reg. 15 in force at 6.2.2018, see reg. 1