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| European Update: CE Labeling Directive Formalizes Requirements |
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Since the implementation of the “New Approach” and the CE Marking in the European Union, the requirements for device labeling have evolved, been reviewed, variously implemented and not uniformly enforced. A closer look at post-market compliance is an evolving trend across many economies. Discussions in the European Union, North America and the Asia-Pacific Economic Cooperation (APEC) continue to focus on post-market surveillance and enforcement. One area of scrutiny, particularly in Europe is device labeling. Council Decision 768/2008, now in effect as of January 1, 2010, formerly implements what should have been done under the existing directive and related decisions. Enforcement and market surveillance has been, in a word, spotty. However, that does not mean the requirements of the directive (now given teeth by the decisions) were not in effect, it only means that not all surveillance agencies were geared up to implement the decision, or if geared up, did not do it. Manufacturers can expect that the ramp-up to full implementation might take sometime. However, it should be understood that it is in effect as of January 1, 2010 and some Member States will begin enforcement as of that date. It would be wise for any manufacturer to make sure that they are, at this moment, in compliance with the new decision. Also, for example, 2001/95/EC (called the safety directive) and 93/465 have been in full implementation for quite some time now. If all of the requirements of the directives and decisions already in existence have been done, then the enforcement brought on by these decisions will not have great affect. If however, the directives and existing decisions have not been adequately followed and conformity to the essential requirements has not been adequately put in place, then you can expect some potentially serious issues beginning January 1, 2010. Specific to the implementations are:
The reason is simple: on January 1, 2010, 93/465 is repealed and is replaced with decision 768/2008 (2008/768/EEC) dealing with the various CE marking modules. This means that as of January 1, 2010 the declaration of conformity and CE marking would have to meet the specifics of Annex III and Annex II of 2008/765 It should be noted that this is not new, as 93/465 had the same CE marking requirements. The only thing ‘new’ is the statement “If the CE marking is reduced or enlarged, the proportions given in the graduated drawing in paragraph 1 shall be respected.” This however, should have been, as we say, a ‘no brainer’ as it was always expected that if the CE marking was reduced in size per 93/465 it was to be directly proportionate to the sample marking in that decision. 2008/765 only makes this abundantly clear. Some Directives do already make this statement clear, such as the R&TTE Directive 1999/5/EC. If a CE Marking followed the pre-existing decision as expected, then this should be of no concern. If however, a responsible party did not follow the previous CE marking decisions, then as of January 1, 2010 they must comply so that all products placed on the market on or after January 1, 2010 would be as stated in 2008/765 and 2008/768. |





