ICH Q10 lays out the broad quality requirements for the modern pharmaceutical quality management system. ICH Q10 incorporates many of the core requirements of Good Manufacturing Practice (GMP) seen in ICH Q7 (“Good Manufacturing Practice Guide for Active Pharmaceutical Ingredients”), and is designed to complement both ICH Q8 (“Pharmaceutical Development”) and ICH Q9 (“Quality Risk Management”).
Use this PDF to embed compliance with all 4 areas of the ICH Q10 standard across your entire product lifecycle, from development and technology transfer to manufacturing and discontinuation.