Review of draft guidance documents - Audit framework for medical devices - Page 1 of 3 - Therapeutic Goods Administration

Introduction

1. What is your name?

Name

2. What is your email address?

3. What is your organisation?

Organisation

4. Do you have any feedback on the Draft guidance - Selection criteria for non-mandatory application audits?

(Required)

5. Do you have any feedback on the Draft Guidance - Medical device application audits - Case management process?

(Required)