View source for Document:ICH ICH E11 Guideline R1 (2017)

<noinclude>{{#set:
|DocReference=ICH  ICH E11 Guideline  R1 (2017)
|DocValidityArea=ICH
|DocScopes=G
|DocName=ICH E11 Guideline
|DocVersion=R1 (2017)
|DocStatus=Current
|DocType=International guideline
|DocLanguage=EN
|DocDescription=CLINICAL INVESTIGATION OF MEDICINAL PRODUCTS IN THE PEDIATRIC POPULATION
|DocRestricted=No
|DocSubmittedBy=Florian Adragna
|DocContributors=
}}</noinclude>

{{DocumentBox
|reference=ICH  ICH E11 Guideline  R1 (2017)
|validity_area=ICH
|scopes=G
|doc_name=ICH E11 Guideline
|version=R1 (2017)
|status=Current
|doc_type=International guideline
|language=EN
|description=CLINICAL INVESTIGATION OF MEDICINAL PRODUCTS IN THE PEDIATRIC POPULATION
|official_link=https://database.ich.org/sites/default/files/E11_R1_Addendum.pdf
|restricted=No
|submitted_by=Florian Adragna
|contributors=
}}

<noinclude>
== References ==
{| class="wikitable"
! Reference !! Scope !! Document part !! Language !! Preview
|-
| [[Reference:ICH ICH E11 Guideline R1 (2017) -]] || G || - || EN || CLINICAL INVESTIGATION OF MEDICINAL PRODUCTS IN THE PEDIATRIC POPULATION
|-
| [[Reference:ICH ICH E11 Guideline R1 (2017) 8]] || G || 8 || EN || 8. GLOSSARY Parental (legal guardian) consent/permission: Expression of understanding and agreement by fully informed parent(s) or legal guardian to permit the investigator/sponsor of a clinical ...
|}
</noinclude>