The New Legislative Framework Revision of the NAWI-D and the MI-D

Similar documents
Safety of Toys Implementing Regulation

EU- T y p e E x a m i n a t i o n C e r t i f i c a t e

EU- T y p e E x a m i n a t i o n C e r t i f i c a t e

NOTIFIED BODY EU-TYPE EXAMINATION CERTIFICATE

NOTIFIED BODY EU-TYPE EXAMINATION CERTIFICATE

NOTIFIED BODY EU-TYPE EXAMINATION CERTIFICATE

The Recast RoHS Directive 2011/65/EU

(Non-legislative acts) DECISIONS

How to survive the MDR

DRAFT. Applicability of the LVD/EMCD/RED to Specific Categories of Products

Recast de la législation européenne et impact sur l organisation hospitalière

Guide to the Radio Equipment Directive 2014/53/EU. Version of 05 June 2018

Guide to the Radio Equipment Directive 2014/53/EU. Version of 19 December 2018

Committee on the Internal Market and Consumer Protection

Machinery ADCO WG on Market Surveillance

Preparing for the new Regulations for healthcare providers

Guide on the General and Administrative Aspects of the Voluntary System of Modular Evaluation of Measuring instruments

COMMUNICATION FROM THE COMMISSION TO THE EUROPEAN PARLIAMENT. pursuant to Article 294(6) of the Treaty on the Functioning of the European Union

Position Paper.

Co-ordination of the Group of Notified Bodies for the Construction Products Directive 89/106/EEC. GNB-CPD Conference on CPR

Application for Assessment of a full quality assurance system regarding Measuring Instruments in accordance with MID

Technical Documentation for CE Marking

1 SERVICE DESCRIPTION

Questions and answers on the revised directive on restrictions of certain dangerous substances in electrical and electronic equipment (RoHS)

Machinery Directive 2006/42/EC

Proposal for a COUNCIL REGULATION. on denominations and technical specifications of euro coins intended for circulation. (recast)

ORGALIME Position. on the Proposal for a

CAMD Transition Sub Group FAQ IVDR Transitional provisions

MONETARY AGREEMENT between the European Union and the Vatican City State (2010/C 28/05)

WG food contact materials

EUROPEAN CENTRAL BANK

GSM R Notes on certification

Ocean Energy Europe Privacy Policy

Technical Note. The NOMAD Project A Survey of Instructions Supplied with Machinery with Respect to Noise

History New and Global approach. Anneke van Spronssen

COMMISSION OF THE EUROPEAN COMMUNITIES

COMMISSION IMPLEMENTING DECISION

Assemblies according to the Pressure Equipment Directive - a consideration provided by the PED-AdCo Group 1 -

LITHUANIAN METROLOGY INSPECTORATE ON IMPLEMENTATION OF THE PROVISIONS OF REGULATION (EC) NO 765/2008

Proposal for a COUNCIL DECISION

REPORT FROM THE COMMISSION. of TO THE ECONOMIC AND FINANCIAL COMMITTEE

The Evolution of Technical Communication in Europe

Having regard to the Treaty on the Functioning of the European Union, and in particular Article 16 thereof,

Taximeters common application Directive 2014/32/EU, annexes I & IX (MI-007)

Decree No.1/2006. (II. 15.) of the Governor of Magyar Nemzeti Bank. on the reproduction of the Hungarian legal tender and the euro

ANCOM s Laboratory for Electromagnetic Compatibility and Radio Equipment Testing

CENTRAL BANK OF MALTA

25 July 2017 Without prejudice [PROVISIONS IN RELATION TO TRADE IN GOODS ALREADY INCLUDED IN THE EU TEXT PROPOSAL FOR THE TRADE IN GOODS CHAPTER]

Measuring Instruments Directive 2014/32/EU Thermal Energy Meters Corresponding Tables OIML R 75:2002

COMMISSION STAFF WORKING DOCUMENT. Implementation Plan. Accompanying the document

AGREEMENT on UnifiedPrinciples and Rules of Technical Regulation in the Republic of Belarus, Republic of Kazakhstan and the Russian Federation

Group of Administrative Co-operation Under the R&TTE Directive. 5 th R&TTE Market Surveillance Campaign on WLAN 5 GHz

Proposal for a REGULATION OF THE EUROPEAN PARLIAMENT AND OF THE COUNCIL

ISO/TR TECHNICAL REPORT. Intelligent transport systems System architecture Privacy aspects in ITS standards and systems

WELMEC European cooperation in legal metrology

clarification to bring legal certainty to these issues have been voiced in various position papers and statements.

The Medical Device Regulation: Transitioning between old and new

Notice from the Federal Ministry of Labour and Social Affairs of May 2011 IIIb

European Regulatory Approach to Orbital / Spectrum Registrations

EU Declaration of Conformity

COUNCIL DIRECTIVE 93/42/EEC. of 14 June concerning medical devices

COCIR SUSTAINABLE COMPETENCE IN ADVANCING HEALTHCARE

L 312/66 Official Journal of the European Union

The RoHS Recast Directive 2011/65/EU

COUNCIL OF THE EUROPEAN UNION. Brussels, 19 May 2014 (OR. en) 9879/14 Interinstitutional File: 2013/0165 (COD) ENT 123 MI 428 CODEC 1299

ORGALIME comments ( ) on. Commission LVD UPDATE.2 Working Document dated

COMMISSION OF THE EUROPEAN COMMUNITIES. Draft COMMISSION DECISION

Radio Equipment Directive and Reconfigurable Radio Systems

EN Official Journal of the European Union L 117/176 REGULATION (EU) 2017/746 OF THE EUROPEAN PARLIAMENT AND OF THE COUNCIL.

CEPT MARKING AND THE R&TTE DIRECTIVE. Lisbon, June 2000

Directive 2011/65/EU (RoHS2): Orgalime s Assessment of Revised FAQ Guidance Document

REPUBLIC OF SAN MARINO

European Law as an Instrument for Avoiding Harmful Interference 5-7 June Gerry Oberst, SES Sr. Vice President, Global Regulatory & Govt Strategy

In any of the abovementioned bands, the allocation of the rights of use of frequencies as announced in the NTFA is exigible.

COUNCIL DIRECTIVE 93/42/EEC. of 14 June concerning medical devices

(Text with EEA relevance)

ERC/DEC/(01)07 EUROPEAN RADIOCOMMUNICATIONS COMMITTEE

A practical Guide to understanding the specific obligations of

Fiscal 2007 Environmental Technology Verification Pilot Program Implementation Guidelines

RADIO SPECTRUM COMMITTEE

Official Journal of the European Union L 21/15 COMMISSION

Decision. On the authorization regime governing mobile satellite service (MSS) systems in the 2 GHz band

Precautionary Principle in Health Protection Policies regarding Electromagnetic Fields (EMF)

EUROPEAN CENTRAL BANK

(ECC/DEC/(07)04) (2007/98/EC)

UNOFFICIAL TRANSLATION

TOOL #21. RESEARCH & INNOVATION

Official Journal of the European Union

Recommended code of good practice for the interpretation of Directive 2006/42/EC on machinery concerning air handling units Second Edition

TÜV SÜD Webinar: The European Radio Equipment Directive 2014/53/EU Questions & Answers

Thank you for the opportunity to comment on the Audit Review and Compliance Branch s (ARC) recent changes to its auditing procedures.

COMMISSION OF THE EUROPEAN COMMUNITIES 98/0191 (COD) Proposal for a EUROPEAN PARLIAMENT AND COUNCIL DIRECTIVE

Ref. Ares(2014) /07/2014

Safety of programmable machinery and the EC directive

ORGALIME Comments on

TECHNICAL AND OPERATIONAL NOTE ON CHANGE MANAGEMENT OF GAMBLING TECHNICAL SYSTEMS AND APPROVAL OF THE SUBSTANTIAL CHANGES TO CRITICAL COMPONENTS.

EU-type examination (Module B) certificate

15890/14 MVG/cb 1 DG G 3 C

CONSOLIDATED VERSION

Transcription:

The New Legislative Framework Revision of the NAWI-D and the MI-D

New roles and obligations Enhanced Traceability Explicit language requirements Page 2

1993 2008 2009 2010 2011 2012 2013 2014 2015 2016 20... Council Directive (CD) 90/384/EEC Non-Automatic Weighing Instruments (NAWI) Council Directive (CD) 2009/23/EC Codified Version of NAWI Directive Decision (D) 768/2008/EC New Legal Framework (NLF) Omnibus Revision of CD 2009/23/EC D 768/2008/EC Council Directive (CD) 2009/23/EC (NAWI) Omnibus Council Directive (CD) 2004/22/EC Measuring Instruments Directive (MID) Omnibus Revision of CD 2004/22/EC Decision (D) 768/2008/EC New Legal Framework (NLF) Omnibus D 768/2008/EC Decision (D) 765/2008/EC on Accreditation & Market Surveillance D 765/2008/EC Revision of Conformity Assessment Modules Conformity Assessment (Module A - H1: Instruments under Legal Control) Page 3

Definitions (Art. 2) Economic operators means the manufacturer, the authorised representative, the importer and the distributor Manufacturer means any natural or legal person who manufactures an instrument or has an instrument designed or manufactured, and markets that instrument under his name or trademark Authorised representative means any natural or legal person established within the Union who has received a written mandate from a manufacturer to act on his behalf in relation to specified tasks Importer means any natural or legal person established within the Union who places an instrument from a third country on the Union market; Distributor means any natural or legal person in the supply chain, other than the manufacturer or the importer, who makes an instrument available on the market EVERYBODY INVOLVED IN THE DELIVERY OF AN INSTRUMENT IS NOW SUBJECT TO THE REGULATION Page 4

Definitions (Art. 2) making available on the market means any supply of an instrument for distribution, or use on the Union market in the course of a commercial activity, whether in return for Payment or free of charge. placing on the market means the first making available of an instrument on the Union market; recall means any measure aimed at achieving the return of an instrument that has already been made available to the end user; withdrawal means any measure aimed at preventing an instrument in the supply chain from being DEFINITIONS INCLUDE POST MARKET ACTIVITIES Page 5

Obligations of manufacturers For the instruments used for legal applications, manufacturers shall ensure that procedures are in place for series production to remain in conformity. Changes in instrument design or characteristics and changes in the harmonised standards or in technical specifications by reference to which conformity of an instrument is declared shall be adequately taken into account When deemed appropriate with regard to the performance presented by an instrument, manufacturers shall carry out sample testing of instruments made available on the market, investigate, and, if necessary, keep a register of complaints, of non-conforming instruments and instrument recalls. SHALL KEEP DISTRIBUTORS INFORMED OF ANY SUCH MONITORING. Page 6

Obligations of manufacturers Manufacturers who consider or have reason to believe that an instrument which they have placed on the market is not in conformity with this Directive shall immediately take the necessary corrective measures to bring that instrument into conformity, to withdraw it or recall it, if appropriate Furthermore, where the instrument presents a risk, manufacturers shall immediately inform the competent national authorities of the Member States in which they made the instrument available to that effect, giving details, in particular, of the noncompliance and of any corrective measures taken. IT IS PROBABLE THAT THESE REPRESENT THE OBLIGATIONS THAT MANUFACTURERS PRESENTLY OPERATE TO. IMPORTANT TO NOTE THAT THEY MUST KEEP DISTRIBUTORS INFORMED OF ANY MONITORING Page 7

Authorised Representative An authorised representative shall perform the tasks specified in the mandate received from the manufacturer. The mandate shall allow the authorised representative to do at least the following: (a) keep the EU declaration of conformity and the technical documentation at the disposal of national surveillance authorities for 10 years after the instrument has been placed on the market; (b) further to a reasoned request from a competent national authority, provide that authority with all the information and documentation necessary to demonstrate the conformity of an instrument; (c) cooperate with the competent national authorities, at their request, on any action taken to eliminate the risks posed by instruments covered by the authorised representative s mandate IT IS FELT THAT THESE OBLIGATIONS EXPLICITLY STATE THE RESPONSIBILITIES THAT MANY AUTHORISED REPRESENTATIVES WILL ALREADY FOLLOW Page 8

Obligation of the Importer Importers shall place only compliant instruments on the Union market. When making an instrument available on the market distributors shall act with due care in relation to the requirements of the Directives. Before placing on the market an instrument importers shall ensure and distributor shall verify compliance of the product and the manufacturer. Where there's evidence or doubt about compliance, the importer shall not place on the market and the distributor shall not make available such instruments. Importers/Distributors shall ensure that, storage or transport conditions do not jeopardize the instruments compliance. Importers/Distributors shall ensure the traceability of the products. Page 9

Obligations of the Importer Importers shall place only compliant instruments on the Union market. Before placing on the market an instrument, importers shall ensure that the appropriate conformity assessment procedure has been carried out by the manufacturer. Where an importer considers or has reason to believe that an instrument is not in conformity with the essential requirements, he shall not place the instrument on the market until it has been brought into conformity. Furthermore, where the instrument presents a risk, the importer shall inform the manufacturer and the market surveillance authorities to that effect. Importers shall ensure that storage or transport conditions do not jeopardise its compliance with the essential requirements set out in Annex I. THE IMPORTER IS RESPONSIBLE AND LIABLE FOR THEIR ECONOMIC OPERATION INCLUDING CHECKING AND VERIFYING COMPLIANCE Page 10

Obligations of the Distributor When making an instrument available on the market distributors shall act with due care in relation to the requirements of this Directive. Before making an instrument available on the market, distributors shall verify that the instrument bears the CE marking and the inscriptions, that it is accompanied by the required documents, and that the manufacturer and the importer have complied with the requirements. Where a distributor considers or has reason to believe that an instrument is not in conformity, he shall not make the instrument available on the market until it has been brought into conformity. Furthermore, where the instrument presents a risk, the distributor shall inform the manufacturer or the importer to that effect as well as the market surveillance authorities. Distributors shall ensure that, storage or transport conditions do not jeopardise its compliance with the essential requirements Page 11

Obligations of the Distributor Distributors who consider or have reason to believe that an instrument which they have made available on the market is not in conformity with this Directive shall make sure that the corrective measures necessary to bring that instrument into conformity, to withdraw it or recall it, if appropriate, are taken Where the instrument presents a risk, distributors shall immediately inform the competent national authorities of the Member States in which they made the instrument available to that effect, giving details, in particular, of the noncompliance and of any corrective measures taken. They shall cooperate with that authority, at its request, on any action taken to eliminate the risks posed by instruments which they have made available on the market. CREATES POSITIVE OBLIGATIONS FOR THE DISTRIBUTOR UNLIKELY THAT THEY WILL BE ABLE TO FULFILL THESE OBLIGATIONS WITHOUT THE SUPPORT OF OTHER ECONOMIC OPERATORS Page 12

All economic operators Economic operators shall, on request, identify the following to the market surveillance authorities: (a) any economic operator who has supplied them with an instrument; (b) any economic operator to whom they have supplied an instrument. Economic operators shall be able to present the information referred to in the first paragraph for a period of 10 years after they have been supplied with the instrument and for a period of 10 years after they have supplied the instrument. CAN SEE A FOCUS ON TRACEABILITY Page 13

Page 14

Language Requirements Instructions and Information Manufacturers shall ensure that the instrument is accompanied by instructions and information in a language which can be easily understood by consumers and other end-users, as determined by the Member State concerned. Declaration of Conformity It shall be translated into the language or languages required by the Member State in which market the instrument is placed or made available Documentation to demonstrate conformity Manufacturers shall, further to a reasoned request from a competent national authority, provide it with all the information and documentation necessary to demonstrate the conformity of the instrument, in a language which can be easily understood by that authority THIS IS LIKELY TO POSE MANY PROBLEMS AND CONCERNS FOR ALL ECONOMIC OPERATORS Page 15

Market Surveillance Where, the market surveillance authorities find that the instrument does not comply with the requirements, they shall without delay require the relevant economic operator to take all appropriate corrective action to bring the instrument into compliance with those requirements, to withdraw the instrument from the market, or to recall it within a reasonable period, commensurate with the nature of the risk, as they may prescribe. Where the market surveillance authorities consider that non-compliance is not restricted to their national territory, they shall inform the Commission and the other Member States of the results of the evaluation and of the actions which they have required the economic operator to take. The economic operator shall ensure that all appropriate corrective action is taken in respect of all the instruments concerned that it has made available on the market throughout the Union. THESE OBLIGATION ALLOW THE FRAMEWORK FOR EASIER AND IMPROVED MARKET SURVEILLANCE CAN FORESEE RAPID ESCALATIONOF MATTERS TO THE COMMISSION Page 16

The Blue Guide Likely to be completed via the SOGS committee which should speed it up Pushing for the use of electronic Declarations of Conformity and other document Important process in which to be involved Page 17

New Roles & Obligations Traceability Languages Market Surveillance Page 18

Thank you