Due to recent changes to regulatory requirements – including ISO 13485, the Medical Device Directive, and IEC 60601-1 – medical device manufacturers are now required to have a documented risk management system in place. Rest assured, implementing basic risk management principles doesn’t have to be a complex task. Learn the simple steps you can take towards compliance by viewing our FREE webinar. In just 45 minutes, you'll learn:

• The basic principles of ISO 14971:2007, and how they are related to other medical device directives and regulations
• How risk management can be implemented in conjunction with quality management systems
• How to include risk management as an integral part of the design, production, and post-production processes
• How to demonstrate a clear understanding of the potential hazards to the end user

Watch this webinar online right now – and receive a link to share it with your colleagues later – by completing the form below. Fields marked with a red asterisk (*) are required.