Need Assistance? 1.888.532.6360

Becoming an Effective
ISO 13485 Auditor 101

Planning an ISO 13485 QMS audit? 

If you will be participating in (or leading) an internal ISO 13485 audit for the first time, you likely have many questions. Oriel STAT A MATRIX has answers. This white paper explains the basics of what you need to know before conducting your first medical device QMS audit.

Use the form to receive your copy of the White Paper »

Download the White Paper

All fields are required

© Oriel STAT A MATRIX. All Rights Reserved. | Site Map | Privacy and Legal