View source for Reference:EU EMA/786433/2022 Annex V – to guidance for the conduct of good clinical practice inspections – Phase I units 15-Nov-2022 2.5-002

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{{:Document:EU EMA/786433/2022 Annex V – to guidance for the conduct of good clinical practice inspections – Phase I units 15-Nov-2022}}

{| class="wikitable gplx-infobox"
|-
! colspan="2" class="gplx-infobox-header" | Reference Details
|-
! Module
| Module 4 — Unit 4.5.2
|-
! Scope
| G
|-
! Document part
| 2.5
|-
! Language
| EN
|-
! Original entry by
| Florian Adragna
|-
! Contributors
| 
|-
! Tags
| [[Glossary:TAG-00018-Inv-die|Investigator]], [[Glossary:TAG-00017-Spo-die|Sponsor]], [[Glossary:TAG-00340-Req-nfo|Requirements]]
|-
! Comment
| Repeated entry: 4.5.2 ++ 2.4.0

Personnel requirements: investigator-sponsor relationship
|}

== Content ==
2.5. Personnel
Points to consider:
[…]
• Relationship of the Investigator with the Sponsor company.
[…]