IMDRF Survey - Use of IMDRF/MDSAP WG/N24 (Medical Device Regulatory Audit Reports) - Page 1 of 1 - Medical devices

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

The IMDRF/MDSAP WG/N24 document provides guidance on the format and content of MDSAP medical device regulatory audit reports. This survey aims to understand how regulatory authorities use the document.

1. Please provide the name of your organisation:

Name of your organisation / jurisdiction (Required)

2. Does your organisation currently use IMDRF/MDSAP WG/N24 for any purpose?

(Required) Yes No

3. How is the document used by your organisation? (select all that apply)

(Required) For MDSAP operational use As a template/benchmark for our own audit/inspection report requirements For training and competency development Informational, for reference only (i.e. no active use) Other (please specify):

Other (please specify):