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Reference:GBR The Medicines for Human Use (Clinical Trials) Regulations 2004 01-May-2004 Schedule 1 Part 2 16.: Difference between revisions

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{{#set:
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|HasDocument=Document:GBR The Medicines for Human Use (Clinical Trials) Regulations 2004 01-May-2004
|has_document=Document:GBR The Medicines for Human Use (Clinical Trials) Regulations 2004 01-May-2004
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|scope=HM
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Part 2
Part 2
16.
16.
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|language=EN
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|tags=TAG-00072-Ins-her ++ TAG-00340-Req-nfo ++ TAG-00017-Spo-die ++ TAG-00018-Inv-die
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|tags_display=[[Glossary:TAG-00072-Ins-her|Insurance]], [[Glossary:TAG-00340-Req-nfo|Requirements]], [[Glossary:TAG-00017-Spo-die|Sponsor]], [[Glossary:TAG-00018-Inv-die|Investigator]]
 
|comment=Indemnity and insurance provision requirements
{{:Document:GBR The Medicines for Human Use (Clinical Trials) Regulations 2004 01-May-2004}}
|content=CONDITIONS AND PRINCIPLES WHICH APPLY TO ALL CLINICAL TRIALS
 
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! colspan="2" class="gplx-infobox-header" | Reference Details
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! Document part
| Schedule 1
Part 2
16.
|-
! Language
| EN
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! Original entry by
| Florian Adragna
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! Contributors
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! Tags (EN)
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== Content ==
CONDITIONS AND PRINCIPLES WHICH APPLY TO ALL CLINICAL TRIALS
[…]
[…]
16.  Provision has been made for insurance or indemnity to cover the liability of the investigator and sponsor which may arise in relation to the clinical trial.
16.  Provision has been made for insurance or indemnity to cover the liability of the investigator and sponsor which may arise in relation to the clinical trial.
}}

Latest revision as of 13:50, 16 July 2026



Document information
Reference GBR The Medicines for Human Use (Clinical Trials) Regulations 2004 01-May-2004
Validity area GBR
Scope(s) HM
Document name The Medicines for Human Use (Clinical Trials) Regulations 2004
Version / Revision 01-May-2004
Status Current
Document type Legal act
Language(s) EN
Description The Medicines for Human Use (Clinical Trials) Regulations 2004
Official source Official link
Restricted access No
Submitted by Florian Adragna
Contributors


Reference Details
Module Module 5 — Unit 5.5.0
Scope HM
Document part Schedule 1

Part 2 16.

Language EN
Original entry by Florian Adragna
Contributors
Tags Insurance, Requirements, Sponsor, Investigator

Content

CONDITIONS AND PRINCIPLES WHICH APPLY TO ALL CLINICAL TRIALS […] 16. Provision has been made for insurance or indemnity to cover the liability of the investigator and sponsor which may arise in relation to the clinical trial.

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