Description
New Regulation for Medical Devices (EU) 2017/745 MDR: General Introduction and Principles. Special requirements for Manufacturers/ Technical Documentation
This 3-Day, 10 Hour training is to provide a general introduction and principles. The course will cover special requirements focused on Manufacturers/ Technical Documentation.
General information:
-The concept and policy behind the Regulation
-The “Life Cycle” approach
-The status (after full implementation on 26 May 2021)
Location
Virtual Classroom
Price or participation fee
$1,695.00 USD
Early Bird - Receive 10% off the original price if register 90 days prior to registration