New Regulation for Medical Devices (EU) 2017/745 MDR: General Introduction and Principles. Special requirements for Manufacturers/ Technical Documentation

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