Medical Devices 2011 - ISO 13485 and medical device quality systems - practical strategies for planning, implementation and beyond

This medical device quality systems training will show how you can design and maintain your quality system to meet requirements to target the US, Canada and EU

Whether you are experienced with your medical device quality system or are taking on the responsibility for the first time, it is a benefit to learn proven strategies from quality professionals with hands-on experience.

This session will discuss how to design and maintain your quality system to meet requirements to target the US, Canada and EU. We will also cover documentation and implementation planning, strategies for selection and interface with certification bodies and auditors, and getting value for your investment. You will learn practical tips to help with post registration maintenance, ongoing or expanded certification, and relationships with registrars and auditors.