ICH guideline

ICH E22 EWG: General Considerations for Patient Preference Studies

ICH guideline · Efficacy Guidelines · Step 3

Key facts

ICH code E22 EWG
Title General Considerations for Patient Preference Studies
Guideline series Efficacy Guidelines
ICH step Step 3
ICH summary (excerpt) This topic was endorsed by the ICH Assembly in June 2023. Further to the ICH Management Committee’s endorsement of the E22 Concept Paper in June 2024, the E22 Guideline aims to optimise the use of patient preference information as input to pharmaceutical product development using a globally harmonised framework and…
File Stakeholder Webinar Meeting Report
File type PDF
File on ich.org database.ich.org

At a glance

  • Yes Full text searchable in Orca1
  • Stakeholder Webinar Meeting Report Files published by ICH
  • None FDA guidance documents based on this guideline

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About ICH guidelines

ICH guidelines harmonise the technical requirements for registering medicines in the ICH regions. Each guideline moves through a five-step process, from concept paper to adoption and implementation by regulators.

Source: International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use (ICH). Guideline summaries are ICH material, reproduced with acknowledgement

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