Search Legislation

Regulation (EC) No 765/2008 of the European Parliament and of the CouncilShow full title

Regulation (EC) No 765/2008 of the European Parliament and of the Council of 9 July 2008 setting out the requirements for accreditation and market surveillance relating to the marketing of products and repealing Regulation (EEC) No 339/93 (Text with EEA relevance)

 Help about what version

What Version

 Help about advanced features

Advanced Features

Close

This is a legislation item that originated from the EU

After exit day there will be three versions of this legislation to consult for different purposes. The legislation.gov.uk version is the version that applies in the UK. The EU Version currently on EUR-lex is the version that currently applies in the EU i.e you may need this if you operate a business in the EU.

The web archive version is the official version of this legislation item as it stood on exit day before being published to legislation.gov.uk and any subsequent UK changes and effects applied. The web archive also captured associated case law and other language formats from EUR-Lex.

Changes to legislation:

There are outstanding changes not yet made to Regulation (EC) No 765/2008 of the European Parliament and of the Council. Any changes that have already been made to the legislation appear in the content and are referenced with annotations. Help about Changes to Legislation

Close

Changes to Legislation

Revised legislation carried on this site may not be fully up to date. Changes and effects are recorded by our editorial team in lists which can be found in the ‘Changes to Legislation’ area. Where those effects have yet to be applied to the text of the legislation by the editorial team they are also listed alongside the legislation in the affected provisions. Use the ‘more’ link to open the changes and effects relevant to the provision you are viewing.

View outstanding changes

Changes and effects yet to be applied to Chapter III Section 2:

Changes and effects yet to be applied to the whole legislation item and associated provisions

  • Ch. 3 Art. 27 repeal by EUR 2019/1020 Regulation
  • Ch. 3 Art. 23 repeal by EUR 2019/1020 Regulation
  • Ch. 3 Art. 16 repeal by EUR 2019/1020 Regulation
  • Ch. 3 Art. 29 repeal by EUR 2019/1020 Regulation
  • Ch. 3 Art. 19 repeal by EUR 2019/1020 Regulation
  • Ch. 3 Art. 17 repeal by EUR 2019/1020 Regulation
  • Ch. 3 Art. 22 repeal by EUR 2019/1020 Regulation
  • Ch. 3 Art. 21 repeal by EUR 2019/1020 Regulation
  • Ch. 3 Art. 15 repeal by EUR 2019/1020 Regulation
  • Ch. 3 Art. 24 repeal by EUR 2019/1020 Regulation
  • Ch. 3 Art. 28 repeal by EUR 2019/1020 Regulation
  • Ch. 3 Art. 26 repeal by EUR 2019/1020 Regulation
  • Ch. 3 Art. 20 repeal by EUR 2019/1020 Regulation
  • Ch. 3 Art. 18 repeal by EUR 2019/1020 Regulation
  • Ch. 3 Art. 25 repeal by EUR 2019/1020 Regulation
  • Art. 2(1) words substituted by S.I. 2019/696 Sch. 33 para. 3(c)(i) (This amendment not applied to legislation.gov.uk. Sch. 33 para. 3(c)(i) substituted immediately before IP completion day by virtue of S.I. 2020/1460, reg. 1(4), Sch. 3 para. 22(3)(a))
  • Art. 2(2) words substituted by S.I. 2019/696 Sch. 33 para. 3(d)(i) (This amendment not applied to legislation.gov.uk. Sch. 33 para. 3(d)(i) substituted immediately before IP completion day by virtue of S.I. 2020/1460, reg. 1(4), Sch. 3 para. 22(3)(b))
  • Art. 2(4) substituted by S.I. 2019/696 Sch. 33 para. 3(e) (This amendment not applied to legislation.gov.uk. Sch. 33 para. 3(e) omitted immediately before IP completion day by virtue of S.I. 2020/1460, reg. 1(4), Sch. 3 para. 3)
  • Art. 2(4) words substituted in earlier amending provision S.I. 2019/696, Sch. 33 para. 3(e) by S.I. 2020/852 reg. 4(2) Sch. 1 para. 1(s)(i) (This amendment not applied to legislation.gov.uk. Sch. 1 para. 1(s)(i) omitted immediately before it comes into force by virtue of S.I. 2020/1460, regs. 1(3), Sch. 4 para. 1(3))

SECTION 2U.K. [F1Market] surveillance framework

Article 17U.K.Information obligations

F21.. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .

2.[F3The Secretary of State must take appropriate measures to] ensure that the public is aware of the existence, responsibilities and identity of national market surveillance authorities, and of how those authorities may be contacted.

Article 18U.K.Obligations F4... as regards organisation

F51.. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .

2.[F6The Secretary of State must] establish adequate procedures in order to:

(a)follow up complaints or reports on issues relating to risks arising in connection with products subject to [F7any relevant enactment];

(b)monitor accidents and harm to health which are suspected to have been caused by those products;

(c)verify that corrective action has been taken; and

(d)follow up scientific and technical knowledge concerning safety issues.

[F83.The Secretary of State may by regulations make such provision as the Secretary of State considers appropriate to ensure that market surveillance authorities have the powers necessary for the proper performance of their duties.

The Secretary of State must entrust market surveillance authorities with the resources and knowledge necessary for the proper performance of their duties.

Regulations made under this paragraph must be made by statutory instrument.

A statutory instrument containing regulations under this paragraph may not be made unless a draft of the instrument has been laid before, and approved by a resolution of, each House of Parliament.]

[F94.Market surveillance authorities must exercise their powers proportionately.]

[F105.The Secretary of State must establish, implement and periodically update the United Kingdom's market surveillance programme setting out the principles as to how market surveillance is to be organised and covering the sectors in which market surveillance is conducted in the United Kingdom. The Secretary of State must make this programme available to the public by way of electronic communication and, where appropriate, by other means.]

6.[F11The Secretary of State] [F12must] periodically review and assess the functioning of F13... surveillance activities [F14by market surveillance authorities]. Such reviews and assessments [F12must] be carried out at least every fourth year and the results thereof [F12must] F15... be made available to the public, by way of electronic communication and, where appropriate, by other means.

Textual Amendments

Article 19U.K.Market surveillance measures

1.Market surveillance authorities [F16must] perform appropriate checks on the characteristics of products on an adequate scale, by means of documentary checks and, where appropriate, physical and laboratory checks on the basis of adequate samples. When doing so they [F16must] take account of established principles of risk assessment, complaints and other information.

Market surveillance authorities may require economic operators to make such documentation and information available as appear to them to be necessary for the purpose of carrying out their activities, and, where it is necessary and justified, enter the premises of economic operators and take the necessary samples of products. They may destroy or otherwise render inoperable products presenting a serious risk where they deem it necessary.

Where economic operators present test reports or certificates attesting conformity issued by an accredited conformity assessment body, market surveillance authorities [F16must] take due account of such reports or certificates.

2.Market surveillance authorities [F17must] take appropriate measures to alert users F18... within an adequate timeframe of hazards they have identified relating to any product so as to reduce the risk of injury or other damage.

They [F17must] cooperate with economic operators regarding actions which could prevent or reduce risks caused by products made available by those operators.

[F193.Where a market surveillance authority decides to withdraw a product manufactured in the United Kingdom, it must inform the economic operator concerned at the address indicated on the product in question or in the documentation accompanying the product.]

4.Market surveillance authorities [F20must] carry out their duties independently, impartially and without bias.

[F215.Market surveillance authorities must observe confidentiality where necessary in order to protect commercial secrets or to preserve personal data pursuant to national legislation, subject to the requirements that:

(a)information be made public under this Regulation to the fullest extent necessary in order to protect the users in the United Kingdom;

(b)the protection of confidentiality shall not prevent the dissemination to market surveillance authorities of information relevant to ensuring the effectiveness of market surveillance activities.]

Article 20U.K.Products presenting a serious risk

1.[F22Market surveillance authorities must] ensure that products which present a serious risk requiring rapid intervention, including a serious risk the effects of which are not immediate, are recalled, withdrawn or that their being made available on [F23the] market is prohibited, and that the [F24Secretary of State] is informed without delay thereof, in accordance with Article 22.

2.The decision whether or not a product represents a serious risk [F25must] be based on an appropriate risk assessment which takes account of the nature of the hazard and the likelihood of its occurrence. The feasibility of obtaining higher levels of safety or the availability of other products presenting a lesser degree of risk [F26does] not constitute grounds for considering that a product presents a serious risk.

Article 21U.K.Restrictive measures

1.[F27Market surveillance authorities must] ensure that any measure taken, pursuant to [F28any relevant enactment], to prohibit or restrict the product's being made available on the market, to withdraw it from the market or to recall it, is proportionate and states the exact grounds on which it is based.

2.Such measures [F29must] be communicated without delay to the relevant economic operator, which [F29must] at the same time be informed of the [F30legal] remedies available F31... and of the time limits to which such remedies are subject.

3.Prior to the adoption of a measure referred to in paragraph 1, the economic operator concerned [F32must] be given the opportunity to be heard within an appropriate period of not less than 10 days, unless such consultation is not possible because of the urgency of the measure to be taken, as justified by health or safety requirements or other grounds relating to the public interests covered by [F33any of the relevant enactments]. If action has been taken without the operator's being heard, the operator [F32must] be given the opportunity to be heard as soon as possible and the action taken [F32must] be reviewed promptly thereafter.

4.Any measure referred to in paragraph 1 [F34must] be promptly withdrawn or amended upon the economic operator's demonstrating that he has taken effective action.

Textual Amendments

Article 22U.K.[F35Notification of serious risk]

[F361.Where a market surveillance authority takes or intends to take a measure in accordance with Article 20 it must immediately notify the Secretary of State of that measure.]

2.If a product presenting a serious risk has been made available on the market, [F37the market surveillance authority] [F38must] notify the [F39the Secretary of State] of any voluntary measures taken and communicated by an economic operator.

3.The information provided in accordance with paragraphs 1 and 2 [F40must] include all available details, in particular the data necessary for the identification of the product, the origin and the supply chain of the product, the related risk, the nature and the duration of the F41... measure taken and any voluntary measures taken by economic operators.

4.For the purposes of paragraphs 1, 2 and 3, the market surveillance [F42authority must notify the Secretary of State through the database containing information relating to market surveillance and product safety established by regulation 33(A1) of the General Product Safety Regulations 2005].

Textual Amendments

F43Article 23U.K.General information support system

. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .

F43Article 24U.K.Principles of cooperation between the Member States and the Commission

. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .

F43Article 25U.K.Sharing of resources

. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .

Article 26U.K.Cooperation with the competent authorities of third countries

1.Market surveillance authorities may cooperate with the competent authorities of third countries with a view to exchanging information and technical support F44... and promoting activities relating to conformity assessment, market surveillance and accreditation.

F45...

F462.. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .

Back to top

Options/Help

Print Options

Close

Legislation is available in different versions:

Latest Available (revised):The latest available updated version of the legislation incorporating changes made by subsequent legislation and applied by our editorial team. Changes we have not yet applied to the text, can be found in the ‘Changes to Legislation’ area.

Original (As adopted by EU): The original version of the legislation as it stood when it was first adopted in the EU. No changes have been applied to the text.

Close

See additional information alongside the content

Geographical Extent: Indicates the geographical area that this provision applies to. For further information see ‘Frequently Asked Questions’.

Show Timeline of Changes: See how this legislation has or could change over time. Turning this feature on will show extra navigation options to go to these specific points in time. Return to the latest available version by using the controls above in the What Version box.

Close

Opening Options

Different options to open legislation in order to view more content on screen at once

Close

More Resources

Access essential accompanying documents and information for this legislation item from this tab. Dependent on the legislation item being viewed this may include:

  • the original print PDF of the as adopted version that was used for the EU Official Journal
  • lists of changes made by and/or affecting this legislation item
  • all formats of all associated documents
  • correction slips
  • links to related legislation and further information resources
Close

Timeline of Changes

This timeline shows the different versions taken from EUR-Lex before exit day and during the implementation period as well as any subsequent versions created after the implementation period as a result of changes made by UK legislation.

The dates for the EU versions are taken from the document dates on EUR-Lex and may not always coincide with when the changes came into force for the document.

For any versions created after the implementation period as a result of changes made by UK legislation the date will coincide with the earliest date on which the change (e.g an insertion, a repeal or a substitution) that was applied came into force. For further information see our guide to revised legislation on Understanding Legislation.

Close

More Resources

Use this menu to access essential accompanying documents and information for this legislation item. Dependent on the legislation item being viewed this may include:

  • the original print PDF of the as adopted version that was used for the print copy
  • correction slips

Click 'View More' or select 'More Resources' tab for additional information including:

  • lists of changes made by and/or affecting this legislation item
  • confers power and blanket amendment details
  • all formats of all associated documents
  • links to related legislation and further information resources