How to Simplify Your Compliance with the New ISO 13485:2016

http://MedicalDevicesGroup.net Jon Speer covers 13485:2016, is the first revision of the standard since 2003, and it represents some major changes including the inclusion of risk management throughout the QMS, greater emphasis on quality management throughout the entire product lifecycle and supply chain, and much more. Specifically you will learn: • What exactly changed in the new ISO 13485:2016 • How leveraging technology can help simplify your compliance • 5 steps to take now to make for a smooth transition