Slide background
Direttiva macchine


Tutti i Documenti presenti nella sezione tematica Impianti

sono elaborati o selezionati dalla nostra redazione su Standards riconosciuti.


Acquista l'Abbonamento




Comments to the final report evaluation of the DM 2006/42/EC

ID 4970 | | Visite: 3470 | Documenti Riservati Direttiva macchinePermalink: https://www.certifico.com/id/4970

Orgalime position paper 13 11 2017

Position paper to the final report evaluation of the DM 2006/42/EC

Orgalime comments to the final report on the evaluation of the Machinery Directive 2006/42/EC

Position Paper 13 November 2017

Orgalime welcomes the Evaluation of the Machinery Directive 2006/42/EC (MD) in the framework of the Commission’s Regulatory Fitness and Performance (REFIT) programme and is pleased to comment on the areas of improvement identified by the consultant, for the purpose of providing support in the evaluation process.

Orgalime represents the engineering industry, which is the largest industrial branch in the EU, with a turnover of around €2,000 billion in 2016. The industry accounts for a quarter of manufacturing output and a third of manufactured exports in the European Union.

In accordance with the consultant’s report, Orgalime firmly believes the Machinery Directive is performing well and has reached its objectives of both providing a high level of safety for machinery users and facilitating the free movement of machinery in the internal market.

The adequate implementation of the Directive in the whole of the EU has helped the EU’s manufacturing industries to remain competitive on the internal and global markets with positive consequences at both economic and social level.

The issues to be addressed which have been highlighted within the Evaluation report are as follows:

1. Adapting the Directive to fit/integrate with the New Legislative Framework

2. Adapting the Directive to ensure suitability for new developments

3. Simplification of risk assessment procedures

4. Improvements to definitions/demarcations between particular types of machinery

5. Improved convergence/harmonisation with other similar Directives/Regulations

6. Ensuring increased/improved inspection and therefore widespread compliance of the Directive

As repeatedly mentioned, keeping an industrial base in Europe will only be possible with a strong and competitive manufacturing industry, at the core of the European economy (see also our core policy statement on the REFIT of the Machinery Directive 2006/42/EC).

To reach the objectives of growth and jobs for the future of Europe, manufacturers need a stable and effective legislative framework. For much of our industry, the Machinery Directive 2006/42/EC is the core piece of product legislation enabling companies to place state of the art and safe machinery on the Single Market. In our view, the legislation is performing as it should. We, therefore, urge decision makers to keep the Directive in its current form with minor modifications, if at all necessary, but not impacting its essential requirements and its basic philosophy.

Fonte: Orgalime

Collegati:

Pin It


Tags: Direttiva macchine Abbonati Direttiva macchine

Articoli correlati

Più letti Direttiva macchine

Giu 26, 2019 56732

Regolamento Prodotti da Costruzione (UE) 305/2011 - CPR

Regolamento CPR (UE) 305/2011 Regolamento (UE) N. 305/2011 del Parlamento Europeo e del Consiglio del 9 marzo 2011 che fissa condizioni armonizzate per la commercializzazione dei prodotti da costruzione e che abroga la direttiva 89/106/CEE del Consiglio (Testo rilevante ai fini del SEE) GU L 88/10… Leggi tutto

Ultimi archiviati Direttiva macchine

UDI
Ago 11, 2020 43

Faq Unique Device Identification (UDI) System

Faq Unique Device Identification (UDI) System EC, 11.08.2020 The existing regulatory framework on medical devices dates back to the 1990s and consists of three Directives. Two new Regulations (Regulation (EU) 745/2017 on medical devices and Regulation (EU) 746/2017 on In Vitro diagnostic medical… Leggi tutto
Lug 20, 2020 93

Regolamento delegato (UE) 2020/1059

Regolamento delegato (UE) 2020/1059 Regolamento delegato (UE) 2020/1059 della Commissione del 27 aprile 2020 che rettifica alcune versioni linguistiche dei regolamenti delegati (UE) n. 1059/2010, (UE) n. 1060/2010, (UE) n. 1061/2010, (UE) n. 1062/2010, (UE) n. 626/2011, (UE) n. 392/2012 e (UE) n.… Leggi tutto
General Safety and Performance Requirements  Annex I  MDR
Lug 08, 2020 136

General Safety and Performance Requirements (Annex I) MDR

General Safety and Performance Requirements (Annex I) in the New Medical Device Regulation Comparison with the Essential Requirements of the Medical Device Directive and Active Implantable Device Directive As compliance with the ‘Essential Requirements (ERs)’ is the keystone for establishing… Leggi tutto
Position Paper Assogastecnici Aprile 2020
Lug 08, 2020 153

Regolamento MD: casi pratici in cui il Distributore non assume il ruolo di Fabbricante

Regolamento UE 2017/745: casi pratici in cui il Distributore non assume il ruolo di Fabbricante del DM Position Paper Assogastecnici A differenza della precedente regolamentazione relativa ai Dispositivi Medici (Direttiva 93/42/CEE), il nuovo Regolamento (UE) 2017/745 identifica e definisce alcune… Leggi tutto