Reference:IMDRF IMDRF – Guidelines - -

Document information
Reference	IMDRF IMDRF – Guidelines -
Validity area	IMDRF
Scope(s)	MD
Document name	IMDRF – Guidelines
Version / Revision	-
Status	N.A.
Document type	Corpus of texts
Language(s)	EN
Description	IMDRF: International Medical Device Regulators Forum IMDRF documents - https://www.imdrf.org/documents/library - Technical documents Global Harmonization Task Force (GHTF) - https://www.imdrf.org/documents/ghtf-final-documents GHTF Study Group 1 - Pre-market Evaluation GHTF Study Group 2 - Post-market Surveillance/Vigilance GHTF Study Group 3 - Quality Systems GHTF Study Group 4 - Auditing GHTF Study Group 5 - Clinical Safety/Performance
Official source	Official link
Restricted access	No
Submitted by	Florian Adragna
Contributors

Reference Details
Module	Module 4 — Unit 4.5.1
Scope	MD
Document part	-
Language	EN
Original entry by	Florian Adragna
Contributors
Tags	Audit, Medical device, Harmonised standard

Content

IMDRF: International Medical Device Regulators Forum ; Global Harmonization Task Force (GHTF) GHTF Study Group 4 – Auditing

https://www.imdrf.org/documents/ghtf-final-documents/ghtf-study-group-4-auditing

No final document (01-Feb-2024), but archived documents available.