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CEN-CENELEC 2012 video message
CEN-CENELEC 2012 video message
Script of the video message: Welcome to the new CEN CENELEC website, which we hope will be a useful source of information for everyone who wants to know about standards -- what they are, why we need them and how to use them. We also want to make it easier for people to learn about how standards are being developed, and how various stakeholders can contribute to this process. For the first time we are bringing together in one place information about the activities of CEN and CENELEC, which -- alongside ETSI -- are the main organisations responsible for developing and defining standards at European level. These European standards apply to all kinds of products and services across a wide range of sectors such as chemicals, construction, energy, food, health and safety, household appliances, machinery and transport -- just to mention a few examples. CEN and CENELEC have already been working closely together for many years, and we now have a common management centre in Brussels, as well as a number of joint committees and working groups. There is also close collaboration between the members of CEN and CENELEC, who are the national bodies and electrotechnical committees responsible for standards in 32 countries: all of the EU member states plus Croatia, Iceland, Norway, Switzerland and Turkey. By having common standards that are the same for all European countries, it means that the single market can work more effectively and it creates a level playing field for business. This <b>...</b>
0:34
DUTCH TRANSLATION QUIZ = Cenelec
DUTCH TRANSLATION QUIZ = Cenelec
DUTCH TRANSLATION QUIZ = Cenelec
0:34
SWEDISH TRANSLATION QUIZ = Cenelec
SWEDISH TRANSLATION QUIZ = Cenelec
SWEDISH TRANSLATION QUIZ = Cenelec
0:34
ITALIAN TRANSLATION QUIZ = Cenelec
ITALIAN TRANSLATION QUIZ = Cenelec
ITALIAN TRANSLATION QUIZ = Cenelec
5:00
Regulating Medical Software - Challenges at European and International Levels
Regulating Medical Software - Challenges at European and International Levels
When is software a medical device? Does it need a CE marking? What are the different regulatory landscapes globally? These are some of the questions which were debated at the COCIR/CEN-CENELEC Workshop on Medical Software, held in Brussels on 12 October 2011. The workshop brought together over 100 representatives coming from Canada, Europe, Japan, the United States and beyond. More information here: www.amiando.com