Regulation 50 Operational matters in relation to approved bodiesF1E1
England, Wales and Scotland
Subject to the terms of its appointment, an approved body must carry out the conformity assessment activities and procedures—
in respect of which the body's approval was given under regulation 46; or
in respect of which the body's notification as a notified body was made.
Where an approved body carries out a conformity assessment procedure, it must do so in accordance with Part 2 of Schedule 4.
An approved body must make provision for a manufacturer to be able to make an appeal against a refusal by the approved body—
to issue a Type examination certificate referred to in Schedule 2; or
to affix, or cause to be affixed, the body's identification number pursuant to regulation 44 (identification number).
Annotations
Textual amendments
- F1
Pt. 4 substituted (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. 21 para. 30 (with Sch. 21 para. 37) (as amended by S.I. 2020/676, regs. 1(1), 2 and S.I. 2020/852, regs. 2(2), 4(2), Sch. 1 para. 1(j)); 2020 c. 1, Sch. 5 para. 1(1)
Extent
- E1
This version of this provision extends to England and Wales and Scotland only; a separate version has been created for Northern Ireland only
Notes on the whole SI
Textual amendments
- F1
- F2
1972 c.68. Section 2(2) was amended by section 27(1)(a) of the Legislative and Regulatory Reform Act 2006 (c.51) and by Part 1 of the Schedule to the European Union (Amendment) Act 2008 (c.7). The enabling powers of section 2(2) were extended by virtue of the amendment of section 1(2) by section 1 of the European Economic Area Act 1993 (c.51).
- F3
Paragraph 1A of Schedule 2 was inserted by section 28 of the Legislative and Regulatory Reform Act 2006 and amended by Part 1 of the Schedule to the European Union (Amendment) Act 2008.