Certification
EN 1090-1
Transform steel and aluminum artifacts
The EN 1090 is destined to change the certification structure for all manufacturers of steel and aluminum products. Today it is already possible to place CE marked products on the market only after having characterized them by carrying out initial type tests (ITT) and after introducing and maintaining a factory production control (FPC).
For the recognition of these activities and therefore of the possibility of marking the verification of a Notified Body (ON) that operates and certifies according to the new CPR (Regulation 305/2011 in force since 1 July 2013) which replaces the CPD 89/106 / EC.
for metal carpentry workshops that work / transform steel for structural use, the CE marking according to UNI EN 1090-1in fact, it replaces the certification process of "Transformation Center" at the Central Technical Service.
More detailed considerations regarding the operation of the Transformation Centers and the role of the Technical Director are deferred to dates closer to the entry into force of UNI EN 1090.
Advantages for the company that certifies itself
- minimization of risks from the initial stages, through the identification of non-conformities that could lead to legal consequences
- easy access to markets through FPC certification, which allows companies to market their CE marked products in EU markets
- obtain wide recognition through certification, thanks to its independence and impartiality
Certification Process
> Request for an offer from the customer interested in certification
> Acquisition of all the information necessary for the certification and issue of the offer by AX-REGISTER
> Acceptance of the offer by the customer
> Analysis of any gaps and assessment of the current compliance of the ISMS with the regulatory requirements
> Verification aimed at evaluating the implementation of the principles and structure of the Management System (applicable legislation and regulations, security policy, risk analysis, Statement of Applicability (SoA), clear and consistent definition of the purpose, risk treatment plan)
> Verification aimed at evaluating the adequate and effective implementation of the Management System, through techniques that involve the analysis of documents, observations, interviews with personnel.
> This verification is aimed at issuing the certificate
> Audit carried out annually after certification, to check continuous improvement
> The Renewal Audit is carried out after three years following a complete verification or continuous evaluation over time.
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