Drug manufacturing, standardization and quality control in homoeopathic pharmacy

Homoeopathic pharmacy forms the scientific foundation of homoeopathic therapeutics by ensuring the safety, quality, and consistency of medicines. The therapeutic efficacy of homoeopathic drugs is intrinsically linked to standardized drug manufacturing processes, precise potentization techniques, and stringent quality control measures. This article provides a comprehensive overview of the sources of homoeopathic drugs, principles of pharmaceutical preparation, processes of trituration and potentization, and modern quality assurance practices in accordance with World Health Organization (WHO) and Good Manufacturing Practice (GMP) guidelines. The role of standardization and emerging analytical approaches in strengthening the scientific credibility of homoeopathic pharmacy is also discussed.