Classifying Medical Devices - US and EU 2017

  • 21 Mar 2017
  • Webinar

Description

Topics
  • 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
Who should Attend
  • 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

Past Events

Important

Please, check "Classifying Medical Devices - US and EU" official website for possible changes, before making any traveling arrangements

Event Categories

Business: E-Business, Finance, Innovations, Internal Audit & Compliance, Marketing & Sales, Quality assurance
Education: E-learning
Health & Medicine: Medical device, Medical laboratories, Medical technology
Technology: Data management

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