ICH: quality

The European Medicines Agency publishes scientific guidelines on human medicines that are harmonised by the International Council for Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use (ICH).

If you have comments on a document which is open for consultation, use the .

For a complete list of scientific guidelines currently open for consultation, see Public consultations.


Analytical validation


Regulatory acceptance

Quality of biotechnological products


Good manufacturing practice

Pharmaceutical development

Lifecycle management

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