ICH guideline

ICH M16 EWG: Structured Product Quality Submissions

ICH guideline · Multidisciplinary Guidelines

Key facts

ICH code M16 EWG
Title Structured Product Quality Submissions
Guideline series Multidisciplinary Guidelines
ICH summary (excerpt) This topic was endorsed by the ICH Assembly in April 2025, and the M16 Working Group has been established to develop a final Concept Paper.
File M16 Work Plan
File type PDF
File on ich.org database.ich.org

At a glance

  • Yes Full text searchable in Orca1
  • M16 Work Plan Files published by ICH
  • None FDA guidance documents based on this guideline

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

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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