<?xml-stylesheet type="text/xsl" href="https://emersonexchange365.com/cfs-file/__key/system/syndication/rss.xsl" media="screen"?><rss version="2.0" xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:slash="http://purl.org/rss/1.0/modules/slash/" xmlns:wfw="http://wellformedweb.org/CommentAPI/"><channel><title>Regulatory Requirements for Medical Devices Webinar</title><link>/industries/lifesciences/b/life-sciences-blog/posts/regulatory-requirements-for-medical-devices-webinar-914422726</link><description>There is a new requirement for medical device companies selling into the European market, called the Medical Device Regulation, or MDR. This new regulation places a focus on the supply chain, meaning suppliers in the industry must have a good understanding</description><dc:language>en-US</dc:language><generator>Telligent Community 13</generator></channel></rss>