The International Council for Harmonisation (ICH): 'E' group of guidelines

Below is the overview of 'E' group of ICH guidelines that collectively apply to different stages and types of pre- / clinical research and development.

ICH: ‘E’ group of guidelines overview
General Considerations for Clinical Studies:	E 8 (R1) ICH Consensus Guideline
Design and Analysis:	E4 Dose-Response Studies
	E9 Statistical principles for Clinical Trials
	E10 Choice of Control Group in Clinical Trials
	E17 Multi-Regional Clinical Trials
Conduct and Reporting:	E3 Clinical Study Reports
Conduct and Reporting:	E6 ICH Good Clinical Practice E6 (R3) ICH Guideline on good clinical practice (GCP) - Step 2b. Draft version text
Safety Reporting:	E1 Clinical Safety for Drugs used in Long-Term Treatment
	E2A – E2F Pharmacovigilance
	E14 Clinical Evaluation of QT
	E19 Safety Data Collection
Populations:	E5 Ethnic Factors
	E7 Clinical Trials in Geriatric Population
	E11 – E11A Clinical Trials in Pediatric Polulations
	E12 Clinical Evaluation by Therapeutic Category
Genetics / Genomics	E15 Definitions in Pharmacogenetics/Pharmacogenomics
	E16 Qualification of Genomic Biomarkers
	E18 Genomic Sampling

Other EU Guidelines:

Guideline for the notification of serious breaches of Regulation (EU) No 536/2014 or the clinical trial protocol

Author: European Medicines Agency

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