MENU
  1. Academy
  2. Medical Devices
  3. MDSAP & Participating Country Regulatory Processes

Course Objectives

The aim of this 1 day course is to provide information and knowledge about the MDSAP & Participating Country Regulatory Processes.

The course will include:

  • Introduction to MDSAP & MDSAP Audit model 
  • Understanding Australian Regulatory requirements
  • Understanding Brazil Regulatory requirements
  • Understanding Canada Regulatory requirements
  • Understanding Japan Regulatory requirements
  • Understanding US FDA Regulatory requirements
  • Understanding the difference between MDSAP Audit and ISO Audit

For more information on MDSAP

Locations

Class Dates

Anaheim, California

February 9, 2018 (Medical Devices Roadshow and MD&M West)

Orlando, Florida

February 21, 2018 (Medical Devices Roadshow)

 

 

Questions?

Katie Lehoullier


Katie Lehoullier joined the TUV USA team in 2016 as Administrative Office Support. Katie assists in the development of TUV USA’s Academy Division as the Training Coordinator.

In order to provide you with a pleasant online experience, we use cookies on our website. By expressing your consent at tuev-nord.de you agree to the use of cookies. Further information, e.g. how you can object to the use of cookies at any time, can be found in our cookie guidelines and data protection settings.