Author profile

Forough Homayonpour

Consultant Quality Assurance

Quality assurance expert in GMP documentation, deviations, CAPA and change control in pharmaceutical and biotechnology manufacturing environments. Several years in operational quality assurance, batch record review and inspection readiness, previously in pharmaceutical quality control; M.Sc. in Bioinformatics and Systems Biology (Justus Liebig University Giessen) and in Cell and Molecular Biology.

Articles by Forough Homayonpour

1 article

ArticleNov 6, 2026

CAPA in a GMP environment: are we fixing the root cause or only the symptom?

Documenting a deviation is mandatory, understanding it is the real work. Without a sufficient investigation of the underlying root cause, there is a risk of taking actions that only treat the symptoms.

Image notice: The illustrative and header images were generated using AI and do not depict real people, places, or events. The portrait photographs show real people.

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