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TORONTO, ON--(Marketwired - August 10, 2017) - In 2016, significant revisions were made to the quality management standard ISO 13485, an internationally recognized standard for all medical device manufacturers. The updated changes to ISO 13485 -- the first since 2003 -- demonstrate the increasing Quality System requirements for the global medical device industry and how organizations must adhere to the forthcoming and revised standard.
During a live broadcast on Thursday, August 31, 2017 at 10am EDT (3pm BST/UK), regulatory expert Linda Mummah Schendel, Principal Medical Research Manager at NAMSA, will discuss the steps that medical device manufacturers should take now to effectively prepare for the new standard by the mandatory implementation date in 2019.
This webinar will highlight best practices, suggestions and other information, including:
For more information or to register for this complimentary event visit: ISO 13485:2016 for Medical Device Manufacturers: Ensuring a Smooth Transition through Effective Preparation
Xtalks, powered by Honeycomb Worldwide Inc., is a leading provider of educational webinars to the global Life Sciences community. Every year thousands of industry practitioners (from pharmaceutical & biotech companies, private & academic research institutions, healthcare centers, etc.) turn to Xtalks for access to quality content. Xtalks helps Life Science professionals stay current with industry developments, trends and regulations. Xtalks webinars also provide perspectives on key issues from top industry thought leaders and service providers.NEXT ARTICLE
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