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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)