CE conformity

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Contact:

Dr. Jürgen Hess 

Senior Account Manager

Tel.:  49 (69) 797-84631

 hess@siemens.com

CE conformity

Qualified consulting with regard to EC directives, e.g. pressure equipment directive, machinery directive

Conformity of a product with EC directives (and corresponding implementation to national laws, as required) and EC regulations is expressed by CE marking.

CE marking is required for all products that

  • are subject to one or more EC Directives or Regulations, that require CE marking, and that

  • are subject to one or more EC Directives or Regulations, that require CE marking, and that

This also applies to majorly modified products that are then subject to one or several EC Directives in the form of new products.

This applies regardless of the product

  • being provided in return for payment or without payment or if it is borrowed

  • being produced in the EU or imported from third countries (non-EU regions)

  • being produced as single pieces or in series

  • having been produced prior to or after coming into force of the respective EC Directive

  • being produced in-house for on-site use or having been purchased


CE-Konformität

Operators of chemical and pharmaceutical plants must also deal with the topics of CE marking and certification procedures.

Compliance with the relevant rules and regulations at early project stages such as planning and design of plants helps preventing high consequential costs due to potential reworking and repair.

Being a professional consulting company with many years of experience in the chemical and pharmaceutical industries, we will assist you in implementation of such requirements as specified e.g. in ATEX, the Machinery Directive or the Pressure Equipment Directive, to ensure regulation-compliant construction of your plant.