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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