On May 1, a European Commission Decision comes into force to ensure that no consumer product containing the strongly sensitising DMF is placed on the market in the EU. The biocide dimethylfumarate (DMF) has caused severe allergic reactions, including skin itching, irritation, redness, burns and, in some cases, acute respiratory difficulties, in hundreds of consumers in the EU because of its use in imported every day consumer products such as couches and shoes. There has even been one case of a soft toy for small children. If already on the market, these products will have to be recalled and withdrawn without delay, and consumers will have to be informed about the serious risk. The Commission Decision is an EU wide emergency measure, pending the adoption of a more permanent regulatory solution.
This example of a fake CE marking took me by complete surprise. I went out with my wife and daughter to a restaurant on the beach in The Hague. We ordered two beers. And look what we found:Read More
The number of dangerous consumer products withdrawn from the EU market rose by 16% in 2008 compared to in 2007, the Commission’s annual report on the Community rapid alert system for non-food dangerous products (“RAPEX”) reveals today. This rise from 1 605 notifications in 2007 to 1 866 last year shows that the capacity of the RAPEX system has substantially increased again in 2008, following a substantial investment of resources and training by the European Commission and Member States. European businesses in the consumer product safety area are also taking their responsibilities more seriously and recall their unsafe products from the market more readily. Toys with childcare articles (such as bicycles, baby walkers, cots and soothers), electrical products and motor vehicles were the most frequently notified products in 2008. The number of notifications on products of Chinese origin sent through RAPEX increased (from 52% in 2007 to 59% in 2008). This must be seen as a consequence of the focus of market surveillance authorities on product categories known to be of higher risk.
The European Commission has published updated lists of European harmonized standards for the Pressure Equipment Directive 97/23/EC. Manufacturers of CE marked pressure equipment should check if the European harmonized standards that they have used during the conformity assessment are still valid, or whether they have been updated by these lists.
The European Commission and EU Member States have decided to lower further the fees payable to the Community agency responsible for granting EU-wide trade mark rights, OHIM (Office for the Harmonization in the Internal Market, located in Alicante, Spain), and to simplify the registration procedure. This measure, which follows an initial reduction in 2005 (IP/05/1289), will make trade mark protection much cheaper and easier to obtain for businesses operating in the EU single market, saving them some €60 million a year. It will come into force on 1 May 2009.
For the last 20 years, there has not been a single week in which I have not been asked the following:
“How much does CE marking cost?”
It is a very understandable question. I am sure that it is on your mind as well. Before you start the process of getting the CE marking, it is good to have an overview of the costs involved. But most people do not realize how difficult it is to answer this question.
Often we get a question similar to this:
“Our product already has a UL and/or CSA approval. Does that mean that we automatically qualify for the CE marking?”
Unfortunately, that is not the case.