CONSULT.ClosedConsultation · gov.uk
Consultation on the International Council for Harmonisation (ICH) M14
Consultation on the ICH E2D(R1) guidelines on General principles on plan, design, and analysis of pharmacoepidemiological studies that utilise real-world data for safety assessment of medicines.
Last fetched 03 May 2026 · gov.uk
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The Medicines and Healthcare products Regulatory Agency (MHRA) became a full member of International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use (ICH) in May 2022 and is consulting with UK stakeholders and ICH members on the ICH E2D(R1) guideline on General principles on plan, design, and analysis of pharmacoepidemiological studies that utilise real-world data for safety assessment of medicines.
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