Classifying Medical Devices - US and EU 2017

Classifying Medical Devices - US and EU 2017 is a webinar that covers topics such as:

• Medical device determination
• Purpose and reason for classifying medical devices
• Medical Device exemptions and when they apply
• The medical device classification panels
• The process of classifying a medical device in the US
• Product code classification database and how it is used
• The impact of the new EU Medical Device Regulation on EU medical device classifications
• The process of classifying a medical device in the EU

Classifying Medical Devices - US and EU 2017 is intended for:

• Audit and Compliance Personnel
• Medical Device industry
• Quality Professionals
• Regulatory Professionals
• Design Engineers
• Risk Managers
• VP, Directors and Managers of medical device design functions
• Research and Development Engineers
• Medical device marketing and sales personnel