Description

This guidance was developed by the appropriate ICH Expert Working Group and was subject to consultation by the regulatory parties, in accordance with the ICH Process. ICH E10 has been implemented by the regulatory bodies of the United States, European Union, Japan, Switzerland and Australia.

Resources

Name	Format	Description	Link
Guidance Document - E10: Choice of Control Group and Related Issues in Clinical Trials	HTML		https://www.canada.ca/en/health-canada/services/drugs-health-products/drug-products/applications-submissions/guidance-documents/international-conference-harmonisation/efficacy/choice-control-group-related-issues-clinical-trials-topic.html
Guidance Document - E10: Choice of Control Group and Related Issues in Clinical Trials	HTML		https://www.canada.ca/fr/sante-canada/services/medicaments-produits-sante/medicaments/demandes-presentations/lignes-directrices/international-conference-harmonisation/efficacite/choix-groupe-temoin-questions-connexes-cadre-essais-cliniques-theme.html

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