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Paragraph 3.2 F1

Under the quality system, each safety component for lifts shall be inspected and appropriate tests as set out in the relevant designated standards or equivalent tests shall be carried out in order to ensure that it meets the conditions referred to in point 1. All the elements, requirements and provisions adopted by the manufacturer shall be documented in a systematic and orderly manner in the form of written policies, procedures and instructions. This quality system documentation shall permit a consistent interpretation of the quality programmes, plans, manuals and records.

It shall contain in particular an adequate description of:

(a)

the quality objectives;

(b)

the organizational structure, responsibilities and powers of the management with regard to product quality;

(c)

the examinations and tests that will be carried out after manufacture;

(d)

the means of monitoring the effective operation of the quality system; and

(e)

the quality records, such as inspection reports and test data, calibration data, reports on the qualifications of the personnel concerned, etc.

Annotations

Textual amendments

F1

Schs. 11-19 inserted (E.W.S.) (31.12.2020) by The Product Safety and Metrology etc. (Amendment etc.) (EU Exit) Regulations 2019 (S.I. 2019/696), reg. 1, Sch. 22 para. 44 (with Sch. 22 para. 37) (as amended by S.I. 2020/676, regs. 1(1), 2); 2020 c. 1, Sch. 5 para. 1(1)