Overview of Medical Device Regulation in Europe 2018

  • 25 Jun 2018
  • Webinar

Description

Overview of Medical Device Regulation in Europe 2018 is a webinar dedicated to to review critical elements of the new regulations and is suitable for clinical, regulatory and quality leaders.

Overview of Medical Device Regulation in Europe 2018 covers topics such as:

  • Regulations and their impact on CERs (Clinical Evaluation Reports)
  • Medical Device Regulation in Europe – background
  • How to design Clinical Trials, including how the MDR will affect post market clinical studies for existing products

Overview of Medical Device Regulation in Europe 2018 intended for:

  • Regulatory affairs
  • Quality managers
  • Clinical managers
  • Manufacturers
  • Project managers
  • Product development managers

Past Events

Important

Please, check "Overview of Medical Device Regulation in Europe" official website for possible changes, before making any traveling arrangements

Event Categories

Business: Innovations, Management, Quality assurance
Education: Training
Health & Medicine: Healthcare, Medical device, Medical technology, Pharma

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