Essential Guide To Clinical Data Collection Under European Medical Device Regulation

Who this guide is for

• Medical device manufacturers who must be well-acquainted with the evolving EU regulations which govern the industry to stay compliant and build a regulatory strategy for success.
• Clinical data professionals who work on medical device studies and must understand how to collect MDR-compliant data.
• Regulatory affairs professionals who seek to improve skills in the regulatory environment for device products with a CE Mark.
• Interested individuals who want to update their knowledge of EU regulatory affairs and clinical trial data collection.

What you’ll learn

• The basics of EU MDR
• Who EU MDR impacts
• When EU MDR takes effect
• EU MDR’s impact on clinical data collection
• How to collect EU MDR-compliant clinical data