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CE marking

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Not to be confused withConsumer electronicsorCouncil of the European Union.

CE marking
Effective regionEuropean Economic Area,Turkey[1]andUnited Kingdom
Effective since1993
Product categoryVarious
Legal statusMandatory
WebsiteCE Marking homepage
CE marking example
CE marking example on a mobile phone charger

The presence of the logoThe letters C and E in a stylised ligature. The E is a lunate epsilon, shaped like a letter C with a horizontal bar.(from French,"conformité européenne"meaning "European conformity" )[2]oncommercial productsindicates that themanufacturerorimporteraffirms the goods' conformity with Europeanhealth, safety, and environmentalprotectionstandards.[3]: 58 It is not a quality indicator or acertification mark.[4]The CE marking is required for goods sold in theEuropean Economic Area(EEA); goods sold elsewhere may also carry the mark.

TheCЄmark indicates that the product may be traded freely in any part of the European Economic Area, regardless of its country of origin. It consists of the CE logo and, if applicable, the four digit identification number of thenotified bodyinvolved in theconformity assessmentprocedure.

Meaning

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TheCЄmark on a product indicates that the manufacturer or importer of that product affirms its compliance with the relevantEU legislationand the product may be sold anywhere in theEuropean Economic Area(EEA). It is a criminal offence to affix aCЄmark to a product that is not compliant or offer it for sale.[5]

For example, most electrical products must comply with theLow Voltage Directiveand theEMC Directive,among others; toys must comply with theToy Safety Directive.(The Low Voltage Directive is about electrical safety; EMC orElectromagnetic Compatibility[6]means the device will work as intended without interfering with, or being affected by, the use or function of any other device.) TheCЄmark indicates compliance with as many norms (directivesandregulations) as apply at the time of the declaration of compliance (see below). In the case of electrical products, several later norms such as theRestriction of Hazardous Substances Directive(RoHS) andWaste Electrical and Electronic Equipment Directive(WEEE) are relevant in addition to the Low Voltage Directive and EMC Directive. The exact significance of theCЄmark therefore depends on when it was applied to a specific unit.

Example of theCЄmark followed by the registration number of a notified body

The marking does not indicate EEA manufacture or that the EU or another authority has approved a product as safe or conformant.[7]The EU requirements may include safety, health, and environmental protection. If stipulated in any EU product legislation, assessment by aNotified Bodyor manufacture according to a certified production quality system may be required. Where relevant, theCЄmark is followed by the registration number of the notified body involved in conformity assessment.

Not all products need CE marking to be traded in the EEA; only product categories subject to relevant directives or regulations are required (and allowed) to bear CE marking. Most CE-marked products can be placed on the market subject only to an internalproduction controlby the manufacturer (Module A; seeSelf-certification,below), with no independent check of the conformity of the product withEU legislation;ANEChas cautioned that, amongst other things, CE marking cannot be considered a "safety mark" for consumers.[8]

Countries requiring the CE marking

[edit]
UKCA mark

CE marking is mandatory for certain product groups intended for sale within the European Union, theEuropean Free Trade Association(EFTA), and Turkey. The manufacturers of products made within these countries, and the importers of goods made in other countries, affirm that CE-marked goods conform to EU standards.

FollowingBrexitin 2020, the UK government proposed to replace theCЄmark with theUKCA marking,with a deadline for replacement of 31 December 2024 in some product categories.[9]For other product categories CE marking acceptance in Great Britain has been indefinitely extended.[10][11]As Northern Ireland (a region of the UK) remained aligned to theEuropean Single Marketunder theNorthern Ireland Protocol,CЄmarking remains mandatory for products placed on the market there, and the UKCA mark is not required.[9]On 1 August, the UK's Department for Business and Trade announced that "The government intends to extend recognition of theCЄmarking for placing most goods on the market in Great Britain, indefinitely, beyond December 2024 ", with" different rules for medical devices, construction products, cableways, transportable pressure equipment, unmanned aircraft systems, rail products, marine equipment and ecodesign ".[10][11]

As of 2019,CЄmarking was not required by countries of theCentral European Free Trade Agreement(CEFTA), but CEFTA members Albania, North Macedonia, Serbia, and Montenegro had applied for membership of the European Union, and were adopting many of its standards within their legislation, as had most Central European former member countries of CEFTA that joined the EU, before joining.

Rules underlying CE marking

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The formal legal status of theCЄmark is set out in variousEU DirectivesandRegulations.[12]The underlying principles are explained in theCommission's "Blue Guide".[3]

Responsibility for CE marking lies with whoever puts the product on the market in the EU, i.e. an EU-based manufacturer, the importer or distributor of a product made outside the EU, or an EU-based office of a non-EU manufacturer.

The manufacturer of a product affixes the CE marking to it but has to take certain obligatory steps before the product can bear CE marking. The manufacturer must carry out aconformity assessment,set up atechnical file,and sign a Declaration stipulated by the leading legislation for the product. The documentation has to be made available to authorities on request.

Importers of products have to verify that the manufacturer outside the EU has undertaken the necessary steps and that the documentation is available upon request. Importers should also make sure that contact with the manufacturer can always be established.

Distributors must be able to demonstrate to national authorities that they have acted with due care and they must have affirmation from the manufacturer or importer that the necessary measures have been taken.

If importers or distributors market the products under their own name, they take over the manufacturer's responsibilities. In this case they must have sufficient information on the design and production of the product, as they will be assuming the legal responsibility when they affix the CE marking.

There are certain rules underlying the procedure to affix the marking:

  • Products subject to certainEU directivesorEU regulationsproviding for CE marking have to be affixed with the CE marking before they can be placed on the market.
  • Manufacturers have to check, on their sole responsibility, which EU legislation they need to apply for their products.
  • The product may be placed on the market only if it complies with the provisions of all applicable directives and regulations and if the conformity assessment procedure has been carried out accordingly.
  • The manufacturer draws up an EU declaration of conformity or a declaration of performance (for Construction Products) and affixes the CE marking on the product.
  • If stipulated in the directive(s) or regulation(s), an authorized third party (Notified Body) must be involved in the conformity assessment procedure or in setting up a production quality system.
  • If the CE marking is affixed on a product, it can bear additional markings only if they are of different significance, do not overlap with the CE marking and are not confusing and do not impair the legibility and visibility of the CE marking.

Since achieving compliance can be very complex, CE-marking conformity assessment, provided by a notified body, is of great importance throughout the entire CE-marking process, from design verification, and set up of the technical file to the EU declaration of conformity.

A guide to the implementation of directives and regulations based on the New Approach and the Global Approach (the "Blue Guide" ) was first published by the European Union in 2000. Updated versions were published on 28 February 2014 and 26 July 2016.[3]

Self-certification

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Depending on the level ofriskof theproduct,the CE marking is affixed to a product by themanufactureror authorized representative who needs to ensure that the product meets all the CE marking requirements. In some cases, if a product has minimal risk, it can be self-certified by a manufacturer making a declaration of conformity and affi xing the CE marking to their own product. Self-certification exists only for products that have a minimal risk for their use, and this is clearly foreseen in the relevant directive and regulation according to the product "category". In order to certify, the manufacturer must do several things:

1. Investigate whether the product needs to have a CE marking. The product must conform to allDirectivesandRegulationsthat apply to the product.
2. Choose theconformity assessmentprocedure from the modules called out by the directive or the regulation for the product according to each category (level of risk) involved. There are several modules available for the Conformity Assessment Procedures, but only a few of them involve self-certification. The most of these procedure require a "type Approval" and a Production conformity assessment by aNotified Body.The common procedures (modules) of certification are as listed below. A product normally needs more than one procedure (Module) to be implemented:
  • Module A– Internal production control.
  • Module B– EC type-examination.
  • Module C– Conformity to type.
  • Module D– Production quality assurance.
  • Module E– Product quality assurance.
  • Module F– Product verification.
  • Module G– Unit verification.
  • Module H– Full quality assurance.
  • Module H1– Full quality assurance and Design Examination.

The level of risk is defined by the "category" of each equipment. The higher the category, the higher the risk. After defining the category, the manufacturer, in order to obtain certification, shall then apply the relevant procedures for the specific category of the product or choose the relevant procedures for a higher-category product. The manufacturer, after insuring that the relevant modules for the product category have been applied, will affix theCЄmark and draw up a Declaration of Conformity. The Declaration of Conformity contains a description of the product, the directive(s) and regulation(s) applied, the product category for each directive or regulation, the module chosen, and the name and registration number of the notified body involved in certification procedures (models).

Notified bodies involved in certification procedures are organizations that have been nominated by amember state(according to anaccreditationprocedure) and have been notified by theEuropean Commission.These notified bodies act as Independent Inspection organizations and carry out the procedures as listed in the relevant Modules applied as stated by the relevant directives and regulations. A manufacturer can choose any notified body (notified for the certain directive or regulation and relevant Modules) in any Member State of the European Union.

In reality, the self-certification process consists of the following stages:

Stage 1: Identify the applicable norm(s)

The first step is to identify whether the product needs to bear CE marking or not. Not all products are required to bear CE marking, only the products that fall within the scope of at least one of the sectoral norms (directives and regulations) requiring CE marking. There are more than 20 sectoral product norms requiring CE marking covering, but not limited to, products such as electrical equipment, machines, medical devices, toys, pressure equipment, PPE, wireless devices and construction products.

Identifying which norm(s) may be applicable, as there may be more than one, involves a simple exercise of reading the scope of each norm to establish which apply to the product (Such as the "Low Voltage Directive," 2014/35/EU). If the product does not fall within the scope of any of the sectoral norm, then the product does not need to bear CE marking (and, indeed, must not bear CE marking).

Stage 2: Identify the applicable requirements of the norm(s)

Each norm has slightly different methods of demonstrating conformity depending on the classification of the product and its intended use. Every Directive or Regulation has a number of 'essential requirements' that the product has to meet before being placed on the market.

The best way to demonstrate that these essential requirements have been met is by meeting the requirements of an applicable 'harmonised standard,’ which offer a presumption of conformity to the essential requirements, although the use of standards usually remains voluntary. Harmonised standards can be identified by searching the 'Official Journal' on the European Commission's website, or by visiting the New Approach website established by the European Commission and EFTA with the European Standardisation Organisations.

Stage 3: Identify an appropriate route to conformity

The process is not always a self-declaration process, there are various 'attestation routes' to conformity depending on the Directive or Regulation and classification of the product. Many products (such as invasive medical devices, or fire alarm and extinguisher systems, Pressure Equipment, Lifts etc.) in most cases, have a mandatory requirement for the involvement of an authorised third party e.g. a "notified body".

There are various attestation routes which include:

  • An assessment of the product by the manufacturer.
  • An assessment of the product by the manufacturer, with additional requirement for mandatory factory production control audits to be carried out by a third party.
  • An assessment by a third party (e.g. EC type test), with the requirement for mandatory factory production control audits to be carried out by a third party.

Stage 4: Assessment of the product's conformity

Example of safety product testing: headphones inanechoic chamber.

When all of the requirements have been established, the conformity of the product to the essential requirements of the norm(s) needs to be assessed. This usually involves assessment and/or testing, and may include an evaluation of the conformity of the product to the harmonised standard(s) identified in step 2.

Stage 5: Compile the technical documentation

Technical documentation, usually referred to as the technical file, relating to the product or range of products needs to be compiled. This information should cover every aspect relating to conformity and is likely to include details of the design, development and manufacture of the product.

Technical documentation will usually include:

  • Technical description
  • Drawings, circuit diagrams and photos
  • Bill of materials
  • Specification and, where applicable, EU declaration of conformity for the critical components and materials used
  • Details of any design calculations
  • Test reports and/or assessments
  • Instructions
  • EU declaration of conformity
  • Technical documentation can be made available in any format (i.e. paper or electronic) and must be held for a period of up to 10 years after the manufacture of the last unit, and in most cases reside in the European Economic Area (EEA).

Stage 6: Make a declaration and affix the CE marking

When the manufacturer, importer or authorised representative is satisfied that their product conforms to the applicable norms, an EU declaration of conformity must be completed or, for partly completed machinery under the Machinery Directive, an ECU declaration of incorporation.[13]

EU declaration of conformity

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The EU declaration of conformity must include: manufacturer's details (name and address, etc.); essential characteristics the product complies; any European standards and performance data; if relevant the identification number of the notified body; and a legally binding signature on behalf of the organization.[14]

Product groups

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CЄmark on personal protective equipment (a glove)
CЄmark on radio equipment (a Wi‑Fi card)
CЄmark on electronic equipment (electronic cigarette)

The norms (directivesandregulations) requiring CE marking affect the following product groups:[15][16]

Mutual recognition of conformity assessment

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There are numerous 'Agreements on Mutual Recognition of Conformity Assessment' between the European Union and other countries such as the US, Japan, Canada, Australia, New Zealand and Israel.[citation needed]Consequently, CE marking is now found on many products from these countries. Japan has its own marking known as the Conformity Mark.[17]

Switzerland and Turkey (which are not members of the EEA) also require products to bear CE marking as an affirmation of conformity.[18][19]

Characteristics of CE marking

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Proportion requirements of the CE marking
  • The CE marking has to be affixed by the manufacturer or its authorized representative in the European Union according to its legal format visibly, legibly and indelibly to the product
  • When a manufacturer puts the CE marking on a product it implies that it complies with all the Essential Health and safety requirements from all the directives and regulations that applies to its product.

When the manufacturer of a machine puts the CE marking, it engages itself and guarantees, that it makes all the tests, assessments and evaluation on the product to conform to all the requirements ofallthe norms that apply to its product.

  • CE marking has been introduced by the COUNCIL DIRECTIVE 93/68/EEC of 22 July 1993 amending Directives 87/404/EEC (simple pressure vessels), 88/378/EEC (safety of toys), 89/106/EEC (construction products), 89/336/EEC (electromagnetic compatibility), 89/392/EEC (machinery), 89/686/EEC (personal protective equipment), 90/384/EEC (non-automatic weighing instruments), 90/385/EEC (active implantable medicinal devices), 90/396/EEC (appliances burning gaseous fuels), 91/263/EEC (telecommunications terminal equipment), 92/42/EEC (new hot-water boilers fired with liquid or gaseous fuels), 93/42/EEC (medical devices) and 73/23/EEC (electrical equipment designed for use within certain voltage limits).
  • The size of the CE marking must be at least 5 mm, if enlarged its proportions have to be kept.
  • If the appearance and workmanship of a product do not allow for the CE marking to be affixed on the product itself, the marking has to be affixed to its packaging or accompanying documents.
  • If a norm requires the involvement of a Notified Body in the conformity assessment procedure, depending on the legislation, an identification number may need to be put behind the CE logo. This is done under the responsibility of the Notified Body.[12]

Misuse

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The European Commission is aware that CE markings, like other certifications marks, are misused.[20]CE marking is sometimes affixed to products that do not fulfill the legal requirements and conditions, or it is affixed to products for which it is not required. In one case it was reported that "Chinese manufacturers were submitting well-engineered electrical products to obtain conformity testing reports, but then removing non-essential components in production to reduce costs".[21]A test of 27electrical chargerswith UK sockets in 2008 found that all the eight legitimately branded ones with a reputable name met safety standards, but none of those unbranded or with minor names did, despite bearing theCЄmark;[21]non-compliant devices were actually potentially unreliable and dangerous, presenting electrical and fire hazards.

There are also cases in which the product complies with the applicable requirements, but the form, dimensions, or proportions of the mark itself are not as specified in the legislation.[20]

"China Export"

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See also:BackronymandChina Compulsory Certificate

In 2008, a logo very similar to CE marking was alleged to exist and to stand forChina Exportbecause some Chinese manufacturers apply it to their products.[22]However, theEuropean Commissionsays that this is a misconception.[20]The matter was raised at theEuropean Parliamentin 2008.[23]The Commission responded that it was unaware of the existence of any "Chinese Export" mark and that, in its view, the misunderstanding had arisen because a producer had failed to respect the precise dimensions and proportions of the mark as prescribed in the legislation.[20]The Commission was also aware of fraudulent misuse of the mark on products that did not comply with the standards, but that this is a separate issue.[20]It had initiated the procedure to register CE marking as a Community collectivetrademark,and was in discussion with Chinese authorities to ensure compliance withEU legislation.[20]Chinese (and other non-EU) manufacturers are permitted to use theCЄmark provided that the goods have been manufactured in accordance with the relevant EU directives and regulations.[20]

Nevertheless, and despite the Commission's assurance that it is without foundation, thisurban mythcontinues to propagate on many websites.[24]

In March 2017, another question was put to the European Commission on the statistics of the fraudulent use of the CE mark, reasserting the "China Export" myth.[25]In reply, the Commission notes that it is the responsibility of Member States to take legal action on infringements; the Commission does not have statistics on the penalties that were imposed by Member States for the improper use of the CE marking.[26]

Domestic plugs and sockets

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Directive 2006/95/EC, the "Low Voltage" Directive, specifically excludes (amongst other things)plugs and socket outlets for domestic usewhich are not covered by any Union norm and therefore must not be CE marked.[27]Throughout the EU, as in other jurisdictions, the control ofplugs and socket outlets for domestic useis subject to national regulations. Despite this, the illegal use of CE marking can be found on domestic plugs and sockets, particularly so-called "universal sockets".[28]

It is fairly common to see domestic sockets (and adaptors) that have an inbuilt 5 volt power supply. In the case of these sockets they must be CE marked, but theCЄmark applies to the 5 volt converteronlyand not the rest of the socket or adaptor. This is comparable to dedicated 5 volt power supplies.

[edit]

There are mechanisms in place to ensure that the CE marking is put on products correctly. Controlling products bearing CE marking is the responsibility of public authorities in member states, in cooperation with theEuropean Commission.Citizens may contact national market surveillance authorities if the misuse of the CE marking is suspected or if a product's safety is questioned.

In the UK, sale of any product that carries aCЄmark that is not so approved, or outside the scope of approval is a specific offence under Section 1 of theTrade Descriptions Act 1968.[29]The seller of such an article is as equally guilty as the manufacturer or importer. Ignorance as to the true status of the sold item is no defence against a prosecution (strict liability). Under the Act, the misrepresentation is that the sold item conforms to a specification that it does not or that there is no such specification to which it can conform.

The procedures, measures and sanctions applying to counterfeiting of the CE marking vary according to the respective member state's national administrative and penal legislation. Depending on the seriousness of the crime, economic operators may be liable to a fine and, in some circumstances, imprisonment. However, if the product is not regarded as an imminent safety risk, the manufacturer may be given an opportunity to ensure that the product is in conformity with the applicable legislation before being forced to take the product off the market.

Use in computer systems

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As of 31 January 2024,the mark does not have aUnicodecode point,nor is one in prospect.[30]According to the Unicode principles, the mark is a typeface choice for the two ordinary upper-case letters, C and E, with a specifickerningarrangement. The exact geometry that constitutes the mark is provided in thevector graphicsdata of theAdobe Illustrator ArtworkandEncapsulated PostScriptfiles available from the European Commission.[31]

See also

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Motor vehicles

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Onmotor vehiclesand related parts, theUnited Nations Economic Commission for Europe's (UNECE) type approval can overrule some EU legislation, so the"emark "or" Emark ",is often seen instead of the CE logo.[32]Unlike the CE logo, the UNECE marks are not self-certified.[33]

Reversed epsilon

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A mark called the 'reversed epsilon' (ɜ) predates the CE mark but continues to be required onaerosol spraysand measuring container bottles.[34][35][a]

Other

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Notes

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  1. ^The mark is not the numberU+00333DIGIT THREEbutU+025CɜLATIN SMALL LETTER REVERSED OPEN E

References

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  1. ^"Turkey - Standards for Trade".7 January 2024.
  2. ^"CENELEC FAQs".Cenelec.eu.Archivedfrom the original on 15 August 2017.Retrieved11 August2023.
  3. ^abcCommission Notice — The ‘Blue Guide’ on the implementation of EU products rules 2016 (2016/C 272/01)
  4. ^VDE Association for Electrical, Electronic & Information Technologies."CE Telephone".Retrieved12 September2020.
  5. ^"How is the CE mark enforced?".CE Marking Association (UK). 15 December 2017.Retrieved23 September2020.
  6. ^"What Does That CE Mark Mean on Your Electronic Products?".Mcs-testequipment. Archived fromthe originalon 22 August 2015.Retrieved7 September2015.
  7. ^"CE marking".5 July 2016.
  8. ^ "Position Paper"(PDF).Anec.eu.Retrieved19 June2018.CE Marking is a legislative requirement. It is not a mark of safety, nor a mark of quality, and has never been intended as a mark for consumers.
  9. ^ab"Businesses to be given UK product marking flexibility".Department for Business, Energy & Industrial Strategy, Government of the United Kingdom, andGrant ShappsMP. 14 November 2022.
  10. ^ab"CE marking guidance".UK Government.1 August 2023.Page will be updated to reflect the changes in due course.
  11. ^abPartridge, Joanna (31 July 2023)."UK to retain EU safety mark in latest Brexit climbdown".The Guardian.ISSN0261-3077.Retrieved1 August2023.
  12. ^ab"Council Directive 93/68/EEC of 22 July 1993 amending Directives 87/404/EEC (simple pressure vessels), 88/378/EEC (safety of toys), 89/106/EEC (construction products), 89/336/EEC (electromagnetic compatibility), 89/392/EEC (machinery), 89/686/EEC (personal protective equipment), 90/384/EEC (non-automatic weighing instruments), 90/385/EEC (active implantable medicinal devices), 90/396/EEC (appliances burning gaseous fuels), 91/263/EEC (telecommunications terminal equipment), 92/42/EEC (new hot-water boilers fired with liquid or gaseous fuels) and 73/23/EEC (electrical equipment designed for use within certain voltage limits)".EU Publications Office. 22 July 1993.Retrieved16 February2021.
  13. ^"Declaration of Conformity Guidance & Template".Your Europe.14 October 2021.Archivedfrom the original on 30 September 2019.Retrieved9 December2021.
  14. ^"Technical documentation and EU declaration of conformity".Your Europe.Retrieved9 December2021.
  15. ^European Commission - Internal Market, Industry, Entrepreneurship and SMEs - Manufacturers
  16. ^EUR-Lex - Regulation (EU) 2019/1009 of the European Parliament and of the Council of 5 June 2019 laying down rules on the making available on the market of EU fertilising products and amending Regulations (EC) No 1069/2009 and (EC) No 1107/2009 and repealing Regulation (EC) No 2003/2003 (Text with EEA relevance)
  17. ^"MIC The Radio Use Website | FAQ on Technical Conformity Mark".Tele.soumu.go.jp. 23 December 2013.Retrieved7 September2015.
  18. ^"EUROPA - European Commission - Growth - Regulatory policy - NANDO".European Commission.Retrieved7 September2015.
  19. ^"Hizmetler".Testroof. Archived fromthe originalon 15 September 2015.Retrieved7 September2015.
  20. ^abcdefg"Answer given by Mr Verheugen on behalf of the Commission".European Parliament. 9 January 2008.Retrieved5 July2020.
  21. ^abBuckinghamshire Trading Standards: What’s in your socket?, 2008.Detailed article on hazards found due to poor-quality AC adapters. "The good news for the consumer is that there appears to be a cheap charger for any make or model of mobile phone, toy or hand-held games consoles that you might require – the bad news is that it could kill you!"
  22. ^CE China Export (mark),archived fromthe originalon 16 October 2010,retrieved11 April2012; CE Marking,archived fromthe originalon 16 August 2012,retrieved11 April2012
  23. ^"Written question - China Export (CE) mark feeding off the reputation of the European Conformité européenne (CE) mark - P-5938/2007".European Parliament. 29 July 2008.Retrieved7 September2015.
  24. ^"Warning: don't get confused between the CE Mark and the China Export Mark".ybw.6 December 2010.,"Warning: Don't get confused between the CE Mark and the China Export Mark. Chinese companies printing close replica of European standards logo on products".awsafety.co.uk.Archived fromthe originalon 14 December 2020.Retrieved31 May2020.and many more.
  25. ^CIOCCA, Matteo; SALVINI, Angelo."Parliamentary question | China Export and the CE marking | E-001822/2017 | European Parliament".europarl.europa.eu.Retrieved13 April2024.
  26. ^"Parliamentary question | Answer to Question No E-001822/17 | E-001822/2017(ASW) | European Parliament".europarl.europa.eu.Retrieved13 April2024.
  27. ^"GUIDELINES ON THE APPLICATION OF DIRECTIVE 2006/95/EC".European Commission. p. 7.Retrieved23 February2015.
  28. ^"Universal sockets are an unsafe solution, says PlugSafe".Voltimum. 10 October 2014.Retrieved23 February2015.
  29. ^"Trade Descriptions Act 1968".The National Archives.Archivedfrom the original on 30 April 2011.Retrieved9 December2021.
  30. ^"Proposed New Characters: The Pipeline".Unicode Consortium.31 January 2024.Retrieved28 February2024.
  31. ^"Internal Market, Industry, Entrepreneurship and SMEs: CE Marking".European Commission.Retrieved30 November2019.
  32. ^Jarvis, Tim."'e' is for Automobile Electronics ".Compliance Engineering. Archived fromthe originalon 6 October 2008.Retrieved28 December2008.
  33. ^"Frequently Asked Questions (FAQ) regarding WP.29"(PDF).Unece.org.Retrieved7 September2015.
  34. ^"Council Directive 75/324/EEC of 20 May 1975 on the approximation of the laws of the Member States relating to aerosol dispensers".European Commission.
  35. ^"Council Directive 75/107/EEC of 19 December 1974 on the approximation of the laws of the Member States relating to bottles used as measuring containers".European Commission.
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