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Accredited certification services for ISO 9001, ISO 14001, OHSAS 18001, ISO 22000/HACCP,
ISO/IEC 27001
 
Notified body for the conformity assessment in the following areas: NWI, lifts, construction products – FPC
 

 
 

Quality - access to success
no. 9 / September 2010





Quality assurance
no. 62 / April – June 2010
 

 
CONFORMITY ASSESSMENT IN MANDATORY AREA

 Why SRAC

SRAC – Designated Body by MEC (The Ministry of Economy and Finance) and MTCT (The Ministry of Transportation, Constructions and Tourism) is notified at the European level and is registered with the identification number ”NB 2003” in the Official Journal of the European Union.

The organizations choosing SRAC conformity assessment services in the mandatory areas, where SRAC is a designated body:

• benefit from the competence of the auditors and experts involved in the certification and surveillance process, which posses a wide experience in the mandatory area;
   
• may choose also the quality management system certification in compliance with ISO 9001:2000, which may be achieved at the same time with the assessment of conformity, leading to reduced costs and an efficient organization of the surveillance, by the means of planning common audits for the quality management system and the mandatory area;
   
• are included in the list with the organizations assessed by SRAC in the mandatory area, publicly available on SRAC website ;
   
• are regularly informed on the evolutions in the conformity assessment in the mandatory area, by accessing SRAC Website, by invitations to the training courses, symposia and conferences organized by SRAC or by purchasing SRAC editorial products.

 Why conformity assessment in madatory area

Every organization placing on the market and/or putting into service products within the mandatory area (Annex 1 of the Law 608/2001) should:

•  identify the European Directives of the New Approach – transposed in the national legislation by technical regulations – applicable to its products;
   
• identify the applicable conformity assessment procedure (self-declaration of conformity, involvement of a designated body for the assessment of testing, inspection or quality management system or a combination thereof);
   
• to determine the dates by which it has to take action;
   
• to identify the Harmonized European Standards applicable to its products;
   
• to ensure the products comply with the standards and all the essential requirements of the applicable Directive(s);
   
• to affix the CE marking on the products and/or their packaging or accompanying documentation, as provided.

The technical regulations, transposing at national level the New Approach Directives, provide for a range of compliance routes for your products and present, usually in a modular format, the available procedures for conformity assessment.

In many cases, the conformity assessment of the products within the scope of the mandatory area require the involvement of a designated (notified) body, as set forth in the Law 608/2001 and the applicable technical regulations.

CE Marking

  • shows the conformity of the product with the essential requirements of the European Directives (national technical regulations)
  • allows the products to be placed on the market
  • facilitates the free movement of goods
  • allows the withdrawal of non-conforming products by the intervention of competent authorities 

CE Marking

  • is not a certification or approval mark issued by a third party
  • is not a marketing or promotion tool
  • is not a quality mark

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