IMDRF Survey - Use of IMDRF/MDSAP WG/N24 (Medical Device Regulatory Audit Reports)

Overview

The International Medical Device Regulators Forum (IMDRF) publishes documents to support global medical device regulatory harmonization and convergence.

IMDRF is seeking feedback on the use of IMDRF/MDSAP WG/N24 FINAL:2015 Medical Device Regulatory Audit Reports. This document describes the format and content of medical device regulatory audit reports used within the Medical Device Single Audit Program (MDSAP). This short survey aims to understand who uses the document, how it is used, and whether continued access via the IMDRF website is important.

The document is currently published on the IMDRF website and is available at:  https://www.imdrf.org/documents/medical-device-regulatory-audit-reports

Why your views matter

Your feedback will help IMDRF understand the extent to which the IMDRF/MDSAP WG/N24 document is relied upon, including any use beyond MDSAP. The outcome will help inform a decision that maintains appropriate access to the document and minimises disruption for users.