New Delhi, India (PressExposure) May 11, 2009 -- TQ VISION, a leading Management System Development and Engineering Consultancy organisation has signed an agreement with ENTE CERTIFICAZIONE MACCHINE (ECM Group, Italy), a specialized engineering consulting organization, with primary focus on CE MARKING AND PRODUCTS CERTIFICATION. ECM is accredited for CE Marking (CE Certification) by the Italian Department of Trade and Industry, and is an EUROPEAN NOTIFIED BODY Number 1282 for EU Directives for product certification.
With this, TQ VISION can now offer exclusive services for Indian Exporters who wish to market their products in European Market to get the "CE Mark" right here with assistance from TQ VISION.
Speaking on the occasion, Mr. Rajeev Arora, Lead Consultant with TQ VISION confirmed that now TQ VISION can give assistance in CE Marking procedure for the Machinery Directive, EMC Directive, Low Voltage Directive, ATEX Directive, R&TTE (RTTE) Directive, Pressure Equipment Directive (PED), Personal Protective Equipment (PPE) Directive, Medical Device Directive, Construction Products Directive, Toys Directive and In Vitro Device Directive.
Mr. Singh, Head of Product Safety Division at TQ VISION also confirmed that ECM will take complete responsibility for CE Marking, CE Certification, Product Safety & Liability of the products in EU. ECM will also acts as the official legal AUTHORIZED REPRESENTATIVE for Indian manufacturers and exporters who intend to or are exporting their products to Europe. ECM can handle all types of product certification including electrical safety (safety testing), product safety, machinery safety, RoHS Compliance, Third Party Inspections & Audits.
ENTE CERTIFICAZIONE MACCHINE is active worldwide and offers a complete range of technical services ensuring that products comply to the CE Mark regulations.
The added advantage for CE Marking by ECM is that it also provide ECM CONFORMITY MARK, which demonstrates that products meet, comply and exceed to the established standards and requirements of excellence in supplement manufacture. Every product in the production line will be then guaranteed to be complete, balanced, and efficacious.
The ECM CONFORMITY MARK is recognized globally, providing to Clients Product(s) the marketing advantage needed to better position the products above their competitors.
The CE Mark, which is affixed to a product or its packaging, is considered proof that a product has met the requirements of the harmonized European standard, or directive. "CE" refers to CommunautÃ© EuropÃ©en. 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.