Keeping
in mind the full requirements of customers, we offer CE
Mark Certification Service. In addition to
this, this service is identified for reliability, timely
completion. Our service is handled by expert's team
who use advanced technique. Europe is a competitive
but prize market, easier to access than ever before.
Too many Indian exporters, especially small and medium
sized enterprises, avoid it because the technical requirements
for entry seem too complicated, too difficult, or too
expensive. Indian manufacturers who have successfully
accessed the European market know that the time to
understand the European system is well worth the effort.
The European Union alone is filled with affluent consumers,
approximately 450 million of them. The European market
is a large area that comprises more than 25 countries.
For the exporter, therefore, Europe as a whole has
become a market whose technical requirements have been
greatly simplified. Before the creation of the European
Union, each country imposed its own technical requirements.
Different standards and conformity assessment procedures
forced exporters to target one or two countries only,
or to forego exporting to Europe altogether. The unification
of these European countries into a European Union,
and the consequent harmonization of laws, standards,
and conformity assessment procedures, changed all that.
Perhaps more importantly, ISO 9001 Certification is used extensively in Europe
as a condition of acceptance of a manufacturer's product or as a means of recognition
of the manufacturer's credibility. It is important to note that a manufacturer
with a quality system in place (such as ISO 9001 QMS) should not automatically
assume that his or her products are CE compliant because of the quality system
alone. The appropriate New Approach Directive(s) will prescribe the correct and
full route to conformity assessment.
The CE Mark, which is affixed to a product or its packaging, is considered a
proof that the product has met the requirements of the harmonized European standard,
or directives; refers to Communauté European. Translated from the French, this
literally means European Community. The European Commission, which administers
the program, describes the CE Mark as a passport for goods to be sold freely
within the internal European market. It is required by law if the product falls
under one of the New Approach Directives. It is not a quality mark, nor is it
a mark for consumers. Intended for Member State authorities, it is the visible
sign to those authorities that your product is in compliance with the New Approach
Directives. All manufacturers are required to affix the CE mark to products that
are governed by New Approach Directives. CE marking on a product indicates to
all authorities that the product is in compliance with the essential health and
safety requirements of all directives that apply to the product. The first step
to compliance is determining which directives apply to the product. A product
may be regulated by more than one directive. The CE mark does not disclose which
directive(s) or standards apply to the product, nor will it indicate the method
of conformity assessment used to bring the product into compliance. This information
is provided by other accompanying documents, such as the Declaration of Conformity.
The Manufacturer or the Authorized Representative affixes the CE marking to the
product. It is not affixed by a Notified Body.
Additional Information:
Delivery Time: 7
days