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).

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


Stability


Analytical validation


Impurities


Regulatory acceptance


Quality of biotechnological products


Specifications


Good manufacturing practice


Pharmaceutical development

Lifecycle management

 

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