Disambiguation evidence for International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use via surface form
"International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use"
Triples (35)
Triples where some other subject referred to this entity
as "International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use".
European Medicines Agency
→
cooperatesWith
→
"International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use"
ⓘ
ICH Assembly
→
partOf
→
"International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use"
ⓘ
ICH Management Committee
→
partOf
→
"International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use"
ⓘ
ICH Management Committee
→
parentOrganization
→
"International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use"
ⓘ
ICH Secretariat
→
partOf
→
"International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use"
ⓘ
ICH Secretariat
→
operatedBy
→
"International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use"
ⓘ
ICH Secretariat
→
parentOrganization
→
"International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use"
ⓘ
ICH Q8 Pharmaceutical Development
→
issuedBy
→
"International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use"
ⓘ
ICH Q9 Quality Risk Management
→
issuedBy
→
"International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use"
ⓘ
ICH E6 Good Clinical Practice
→
issuedBy
→
"International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use"
ⓘ
ICH E2A Clinical Safety Data Management
→
developedBy
→
"International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use"
ⓘ
ICH M4 Common Technical Document
→
developedBy
→
"International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use"
ⓘ
ICH S9 Nonclinical Evaluation for Anticancer Pharmaceuticals
→
developedBy
→
"International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use"
ⓘ
ICH Q10 Pharmaceutical Quality System
→
issuedBy
→
"International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use"
ⓘ
ICH Q1 Stability Testing of New Drug Substances and Products
→
issuedBy
→
"International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use"
ⓘ
ICH Q3A Impurities in New Drug Substances
→
issuedBy
→
"International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use"
ⓘ
ICH E8 General Considerations for Clinical Trials
→
issuedBy
→
"International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use"
ⓘ
ICH Working Groups
→
partOf
→
"International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use"
ⓘ
ICH Articles of Association amendments
→
appliesTo
→
"International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use"
ⓘ
ICH Secretariat
→
partOf
→
"International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use"
ⓘ
linked to:
Secretariat
ICH Executive Director
→
employer
→
"International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use"
ⓘ
ICH Articles of Association
→
governs
→
"International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use"
ⓘ
ICH Rules of Procedure
→
appliesTo
→
"International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use"
ⓘ
ICH Q11 Development and Manufacture of Drug Substances
→
issuedBy
→
"International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use"
ⓘ
Pharmaceuticals and Medical Devices Agency
→
cooperatesWith
→
"International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use"
ⓘ
ICH CTD
→
developedBy
→
"International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use"
ⓘ
Common Technical Document
→
developedBy
→
"International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use"
ⓘ
Swissmedic
→
cooperatesWith
→
"International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use"
ⓘ
ICH M3(R2) Nonclinical Safety Studies for the Conduct of Human Clinical Trials and Marketing Authorization for Pharmaceuticals
→
issuedBy
→
"International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use"
ⓘ
ICH S6 Preclinical Safety Evaluation of Biotechnology-Derived Pharmaceuticals
→
issuedBy
→
"International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use"
ⓘ
PMDA Japan
→
memberOf
→
"International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use"
ⓘ