By Julian Hodgson
E-book via Hodgson, Julian
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Quality is shown in some of the modules, but a common mistake for some ISO 9000 quality-certified companies is to assume that they can select a module that utilizes ISO 9000 when this is not possible unless the primary directive allows it. There is no mention of ISO 9000 quality in the LVD, EMC, and Machinery directives (see Product Quality versus Factory Quality in Chapter 5). , medical products) under the Medical Device Directive (MDD). ISO 9000 Quality is for companies and factories, it does not cover product safety or EMC conformity!
Where the Commission concludes that the measure is not justified, it shall immediately inform the member state that initiated the action. Member states may adopt "emergency measures" when a product poses a serious and immediate risk. In this case the Commission, with the assistance of a Safety Committee, and the member state cooperate to expedite the actions according to the urgency of the matter. The Committee's opinion shall be delivered to the Commission in a timely matter not to exceed one month.
Compliance with the harmonized standards will, in most cases, ensure a product's conformity with the essential requirements of the directives. Adherence to European harmonized standards is the only proven and universally accepted method of showing conformity with the ERs of the directives (Figure 3-1). " ^ A "presumption of conformity" is conferred by the use of harmonized standards. Products will not benefit from a presumption of conformity when harmonized standards are not properly applied. European standards (norms), are usually based on lEC standards.