Management Review

Training Benefits will include:


1. Understanding the regulatory requirements

2. Defining management responsibilities

3. Implementing controlled systems for completing all requirements

4. The annual management review format

5. Routine interim review

6. Data to provide for management review

7. Integrating risk management

8. Linking the audit systems to management review

9. Managing management review actions

10. Resolving resource issues

11. Highlighting new regulatory requirements

12. Linking Management Review to the CAPA system 


Every participant will have the opportunity to identify key requirements in advance of the course.

Free follow up consultation will be available post training from your course tutor. 

Who should attend?

Personnel in Quality, Design, Regulatory, Engineering, Operations and Suppliers to the medical device industry who are responsible for managing, implementing and using Medical Device Systems which may be subject to FDA inspection.


Contact Details

Incra Med LTD,
Unit 204 Business Innovation Centre,
NUI Galway,
Upper Newcastle,
Galway, Ireland.
Phone: 087 2823571