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Reference:ISO ISO 14155 - Clinical investigation of medical devices for human subjects 2020 Annex A A.17: Difference between revisions

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|RefLanguage=EN
|RefLanguage=EN
|RefTagsEN=
|RefTags=TAG-00075-Pub-ich ++ TAG-00265-Cli-tud ++ TAG-00203-Cli-lin ++ TAG-00201-Cli-eSt
|RefTagsOriginal=
|RefModule=6
|RefTagsFR=
|RefUnit=6.5.0
}}
}}


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! colspan="2" class="gplx-infobox-header" | Reference Details
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| Module 6 — Unit 6.5.0
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! Scope
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! Tags (EN)
! Tags
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| [[Glossary:TAG-00075-Pub-ich|Publication]], [[Glossary:TAG-00265-Cli-tud|ClinicalTrials.gov]], [[Glossary:TAG-00203-Cli-lin|Investigation plan]], [[Glossary:TAG-00201-Cli-eSt|Clinical investigation]]
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Revision as of 17:29, 15 July 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
Module Module 6 — Unit 6.5.0
Scope MD
Document part Annex A

A.17

Language EN
Original entry by Florian Adragna
Contributors
Tags Publication, ClinicalTrials.gov, Investigation plan, Clinical investigation
Comment Publication policy and trial registration statement in CIP

Content

A.17 Publication policy […]

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