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Please use this identifier to cite or link to this item: http://aohindia.in/xmlui/handle/123456789/1730
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dc.date.accessioned2019-04-05T11:26:35Z-
dc.date.available2019-04-05T11:26:35Z-
dc.date.issued2017-
dc.identifier.citationIndian Journal of Research In Homoeopathy Vol.11 (2)en_US
dc.identifier.urihttp://aohindia.in:8080/xmlui/handle/123456789/1730-
dc.description.abstractThe first World Integrated Medicine Forum on the regulation of homoeopathic medicinal products included 50 delegates from 25 countries to discuss the current state of regulation of homoeopathic medicinal products (HMPs). The stakeholders in attendance included government officials, manufacturers, pharmacopoeia organisations, pharmacists, and healthcare providers worldwide. The Minister of Ayurveda, Yoga, Unani, Siddha and Homoeopathy from India, who is likely the only high ranking national official in the world specifically dedicated to oversight of traditional medicines including Homoeopathy, was the keynote speaker for the meeting. The core presentations delivered information on the country‑to‑country variance in regulatory requirements for homoeopathic medicine manufacture and marketing. Different speakers addressed the current pharmacopeia structures in various countries, variance in premarket approval process, regulatory frameworks for homoeopathic medicines, labelling requirements, safety requirements, marketing approaches and good manufacturing practices. Debates focused on quality control testing, stability of intermediate stocks, shelf life of finished products, pre‑market approval process and labelling and they shed light on regional differences in regulation. A lengthy discussion was held on the potential value of harmonisation of pharmacopoeias, manufacturing standards, safety evaluation and labelling. The group consensus was to meet again to pursue specific topics. Daily summaries of take‑away points are provided at the end of each day’s talk summaries. Much acclaim was won by the organisers for materialising this unique forum which proved to be an apt platform for rigorous discussions on lesser discussed, but very vital points such as regulations of HMPs, harmonisation of pharmacopeias and linking industry and regulators’ sectors for unified efforts for global development of Homoeopathy.en_US
dc.description.sponsorshipCCRHen_US
dc.language.isoenen_US
dc.subjectCentral Council for Research in Homoeopathyen_US
dc.subjectDrug regulationsen_US
dc.subjectExport and import of homoeopathic medicinesen_US
dc.subjectGood manufacturing practicesen_US
dc.subjectHomoeopathic industryen_US
dc.subjectHomoeopathic medicinal productsen_US
dc.subjectHomoeopathic pharmacopoeiaen_US
dc.subjectWorld Integrated Medicine Forumen_US
dc.subjectQuality assuranceen_US
dc.titleWorld Integrated Medicine Forum on the regulation of homoeopathic medicinal products: National and Global strategiesen_US
dc.typeArticleen_US
Appears in Collections:Indian Journal of Research in Homoeopathy

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