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Reference:ISO ISO 14155 - Clinical investigation of medical devices for human subjects 2020 7.4.3-001: Difference between revisions

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== Document Information ==
{{:Document:ISO ISO 14155 - Clinical investigation of medical devices for human subjects 2020}}
{{:Document:ISO ISO 14155 - Clinical investigation of medical devices for human subjects 2020}}


== Reference Details ==
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|-
! scope="row" style="width:200px;" | Scope
! colspan="2" class="gplx-infobox-header" | Reference Details
|-
! Scope
| MD
| MD
|-
|-
! scope="row" style="width:200px;" | Document part
! Document part
| 7.4.3
| 7.4.3
|-
|-
! scope="row" style="width:200px;" | Language
! Language
| EN
| EN
|-
|-
! scope="row" style="width:200px;" | Original entry by
! Original entry by
| Florian Adragna
| Florian Adragna
|-
|-
! scope="row" style="width:200px;" | Contributors
! Contributors
|  
|  
|-
|-
! scope="row" style="width:200px;" | Tags (EN)
! Tags (EN)
|  
|  
|-
|-
! scope="row" style="width:200px;" | Tags (original language)
! Tags (original language)
|  
|  
|-
|-
! scope="row" style="width:200px;" | Tags (FR)
! Tags (FR)
|  
|  
|-
|-
! scope="row" | Comment
! Comment
| Repeated entry: 3.4.2 ++ 5.4.2
| Repeated entry: 3.4.2 ++ 5.4.2


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== Text ==
== Content ==
7.4.3 Device deficiencies
7.4.3 Device deficiencies
[…]
[…]

Revision as of 14:27, 29 June 2026



Document information
Reference ISO ISO 14155 -

Clinical investigation of medical devices for human subjects 2020

Validity area ISO
Scope(s) MD
Document name ISO 14155 -

Clinical investigation of medical devices for human subjects

Version / Revision 2020
Status Current
Document type International guideline
Language(s) EN
Description ISO 14155:2020

Clinical investigation of medical devices for human subjects — Good clinical practice

Official source Official link
Restricted access Yes
Submitted by Florian Adragna
Contributors


Reference Details
Scope MD
Document part 7.4.3
Language EN
Original entry by Florian Adragna
Contributors
Tags (EN)
Tags (original language)
Tags (FR)
Comment Repeated entry: 3.4.2 ++ 5.4.2

Device deficiencies: documentation requirements throughout investigation

Content

7.4.3 Device deficiencies […]