View source for Reference:ISO ISO 14155 - Clinical investigation of medical devices for human subjects 2020 7.4.3-001

{{ReferenceData
|has_document=Document:ISO ISO 14155 - Clinical investigation of medical devices for human subjects 2020
|module=3
|unit=3.4.2
|scope=MD
|doc_part=7.4.3
|language=EN
|entry_by=Florian Adragna
|contributors=
|tags=TAG-00208-Dev-ers ++ TAG-00343-Doc-ten ++ TAG-00017-Spo-die ++ TAG-00215-Cor-ahm ++ TAG-00213-Ser-wie
|tags_display=[[Glossary:TAG-00208-Dev-ers|Device deficiency]], [[Glossary:TAG-00343-Doc-ten|Documentation]], [[Glossary:TAG-00017-Spo-die|Sponsor]], [[Glossary:TAG-00215-Cor-ahm|CAPA]], [[Glossary:TAG-00213-Ser-wie|Serious incident]]
|comment=Repeated entry: 3.4.2 ++ 5.4.2

Device deficiencies: documentation requirements throughout investigation
|content=7.4.3 Device deficiencies
[…]
}}