lne.eu
Certified products and companies by LNE
http://www.lne.eu/en/certification/companies-products-certified.asp
Certification Companies and products certified. Companies and products certified. You can find all the public certificates (Products) issued by LNE by questioning our search engine certificates. 2 types of research are available :. By System, Domain, Client name, Certificate number, Effective date . Ask our search engine certificates. Certificats ACERMI et Keymark for thermal insulation products. Accreditation, approval, quality systems. Household products and equipment. Sports and leisure activities.
webinars.lne.eu
Russia Medical Device Market Access, ISO 13485, and CE Marking for Medical Device Manufacturers
http://webinars.lne.eu/medical/russia/index.asp
Russia Medical Device Market Access, ISO 13485, and CE Marking for Medical Device Manufacturers. Russia Medical Device Market Access, ISO 13485, and CE Marking for Medical Device Manufacturers. Join LNE/G-MED and Alexey Stepanov, Regulatory and Quality Assurance Manager Russia and CIS at Sorin Group to have a clear view on the Russian medical device registration process, as well as how to leverage your current product submissions to make your Russian application less labor-intensive. In accordance with F...
webinars.lne.eu
CE Marking and the Roles of Notified Bodies
http://webinars.lne.eu/medical/CE-marking-NB/index.asp
CE Marking and the Roles of Notified Bodies. CE Marking and the Roles of Notified Bodies. Have you ever wondered how the European Directives were made? What does CE stand for? Or Why do we call Notified Bodies by this name and what their role is? View an extract of the webinar. Mise à jour nécessaire. Pour lire la vidéo, vous devez mettre à jour votre navigateur ou votre plugin Flash. To watch entire webinar register. These boxes must be filled in. To keep informed on LNE news and on recent market regula...
webinars.lne.eu
Webinars LNE - Regulatory developments, normatives changes...
http://webinars.lne.eu/index.asp
Our webinars, a free and easy way to review regulatory developments, to be informed on normative changes or to discover new services from your home. Clinical and Performance evidence requirements in the future EU IVD Regulation. Certification Project Manager - LNE/G-MED. Http:/ webinars.lne.eu/medical/clinical-performance-EU-IVD-Regulation/index.asp" class="mail" Share by e-mail. Evolution of ISO 13485:2016 and ISO 9001:2015 standards. Technical Department Director - LNE/G-MED. Consumer products June 2016.
webinars.lne.eu
Optimization of cosmetic packaging : Interactions between container and content
http://webinars.lne.eu/consumer-products/cosmeto-container-content/index.asp
Optimization of cosmetic packaging : Interactions between container and content. Optimization of cosmetic packaging : Interactions between container and content. During this webinar, the following issues will be discussed:. The phenomena of transfer of substances of packaging materials towards cosmetics. The limits of the approach by analyses of migration of substances. The approach by modelling of the transfers of substances. Patrick SAUVEGRAIN R&D Coordinator / LNE. View an extract of the webinar.
webinars.lne.eu
Webinar : Medical devices intended for home use: what are the requirements of EN 60601-1-11 ?
http://webinars.lne.eu/medical/dm-domicile-60601-1-11/index.asp
Medical devices intended for home use: what are the requirements of EN 60601-1-11? Medical devices intended for home use: what are the requirements of EN 60601-1-11? Electrical security requirements for medical electrical devices and systems for home healthcare environments are defined in the first edition of IEC 60601-1-2 and are still not widely known. This collateral standard is used jointly with the general standard EN 60601-1 on the electrical security for medical electrical devices. Prior to this, ...
webinars.lne.eu
Reclassification of Medical Devices, upcoming revisions of EU regulations
http://webinars.lne.eu/medical/reclassification-MD/index.asp
Reclassification of Medical Devices, upcoming revisions of EU regulations. Reclassification of Medical Devices, upcoming revisions of EU regulations. In this webinar, we will analyze the positions of the three main actors (EU Commission / Parliament / Council), focusing on the potential changes affecting the classification of MD and IVD devices. The topics covered in this webinar include:. The state of the EU regulations and the processes it entails. The evolution of the EU regulations. The state of the ...
webinars.lne.eu
Sampling Medical Devices for Testing during Unannounced Audit
http://webinars.lne.eu/medical/sampling-MD-UA/index.asp
Sampling Medical Devices for Testing during Unannounced Audit. Sampling Medical Devices for Testing during Unannounced Audit. Systematic unannounced audit are now broadly implemented following the European Directives requirements and Recommendation 2013/473/EU. One of the provisions of the Recommendation relates to the sampling Notified Bodies could perform during their unannounced audits. As a leading notified body, LNE/G-MED will cover the following topics during this webinar:. Mise à jour nécessaire.
webinars.lne.eu
Webinar : Changes in certification standards
http://webinars.lne.eu/all-sectors/iso-9001-14001/index.asp
Changes in certification standards iso 9001:2015 and iso 14001:2015. Changes in certification standards iso 9001:2015 and iso 14001:2015. The international standards for management systems ISO 9001 and ISO 14001 are the most popular and widely recognised and it is estimated that more than one million certified organisations exist worldwide nowadays. To help you upgrade your management systems to the 2015 versions, we invite you to attend our webinar, which includes:. Q&A session with our experts. Stéphan...