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Future development of global regulations of Chinese herbal products.
J Ethnopharmacol. 2012 Apr 10; 140(3):568-86.JE

Abstract

ETHNOPHARMACOLOGICAL RELEVANCE

GP-TCM is the first EU-funded Coordination Action consortium dedicated to traditional Chinese medicine (TCM) research. One of the key deliverables of the Work Package 7 in GP-TCM was to investigate information of the existing requirements for registration of TCM products listed by global regulatory bodies. The paper aims to collate data and draw comparison of these regulations. Case studies are also presented to illustrate the problems involved in registering TCM products in different regions worldwide.

MATERIALS AND METHODS

A collaborative network task force was established during the early stage of the GP-TCM project and operated through exchanges, teleconferences and focused discussions at annual meetings. The task force involved coordinators, academics who are actively involved with R&D of Chinese herbal medicines, experts on monographic standards of Chinese materia medica, representatives from regulatory agencies, experts from industries in marketing Chinese medicines/herbal medicines and natural products. The co-ordinators took turns to chair teleconferences, led discussions on specific issues at AGM discussion sessions, at joint workshops with other work-packages such as WP1 (quality issues), WP3 (toxicology issues) and WP6 (clinical trial issues). Collectively the authors were responsible for collating discussion outcomes and updating written information.

RESULTS

A global overview of regulations on herbal registration has been compiled during the three years of the consortium. The regulatory requirements for registration of herbal products in the EU and China were compared, and this is extended to other regions/countries: Africa, Australia, Brazil, Canada, Japan, Russia, South Korea, Taiwan, and the United States. A wide variation of the regulations for the categories of herbal products exists: food (functional food, novel foods, dietary food for special medical purpose, foods for particular nutritional use, food supplement); cosmetic, traditional herbal medicine products; herbal medicines for human use and veterinary use.

CONCLUSION

The regulatory issues for registration of herbal products are complicated among the countries and regions worldwide. The information summarised in the text is for reference only. Some regulations which are presented in this review are still in legislation process and may change in due course. Before taking any regulatory action, readers are advised to consult current official legislation and guidance and/or to seek appropriate professional advice. The lessons learnt from global regulation of TCM will provide valuable insights for regulation of other traditional medicine such as Ayurveda and Unani medicine, as well as other forms of indigenous medicine. The WHO is well placed to co-ordinate a consultation process with the aim of putting forward suggestions for harmonisation to key regulatory agencies.

Authors+Show Affiliations

Department of Pharmacology, University of Cambridge, UK. tpf1000@cam.ac.ukNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info available

Pub Type(s)

Comparative Study
Journal Article
Review

Language

eng

PubMed ID

22373513

Citation

Fan, Tai-Ping, et al. "Future Development of Global Regulations of Chinese Herbal Products." Journal of Ethnopharmacology, vol. 140, no. 3, 2012, pp. 568-86.
Fan TP, Deal G, Koo HL, et al. Future development of global regulations of Chinese herbal products. J Ethnopharmacol. 2012;140(3):568-86.
Fan, T. P., Deal, G., Koo, H. L., Rees, D., Sun, H., Chen, S., Dou, J. H., Makarov, V. G., Pozharitskaya, O. N., Shikov, A. N., Kim, Y. S., Huang, Y. T., Chang, Y. S., Jia, W., Dias, A., Wong, V. C., & Chan, K. (2012). Future development of global regulations of Chinese herbal products. Journal of Ethnopharmacology, 140(3), 568-86. https://doi.org/10.1016/j.jep.2012.02.029
Fan TP, et al. Future Development of Global Regulations of Chinese Herbal Products. J Ethnopharmacol. 2012 Apr 10;140(3):568-86. PubMed PMID: 22373513.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Future development of global regulations of Chinese herbal products. AU - Fan,Tai-Ping, AU - Deal,Greer, AU - Koo,Hoi-Lun, AU - Rees,Daryl, AU - Sun,He, AU - Chen,Shaw, AU - Dou,Jin-Hui, AU - Makarov,Valery G, AU - Pozharitskaya,Olga N, AU - Shikov,Alexander N, AU - Kim,Yeong Shik, AU - Huang,Yi-Tsau, AU - Chang,Yuan Shiun, AU - Jia,William, AU - Dias,Alberto, AU - Wong,Vivian Chi-Woon, AU - Chan,Kelvin, Y1 - 2012/02/25/ PY - 2011/12/19/received PY - 2012/02/10/revised PY - 2012/02/10/accepted PY - 2012/3/1/entrez PY - 2012/3/1/pubmed PY - 2012/8/2/medline SP - 568 EP - 86 JF - Journal of ethnopharmacology JO - J Ethnopharmacol VL - 140 IS - 3 N2 - ETHNOPHARMACOLOGICAL RELEVANCE: GP-TCM is the first EU-funded Coordination Action consortium dedicated to traditional Chinese medicine (TCM) research. One of the key deliverables of the Work Package 7 in GP-TCM was to investigate information of the existing requirements for registration of TCM products listed by global regulatory bodies. The paper aims to collate data and draw comparison of these regulations. Case studies are also presented to illustrate the problems involved in registering TCM products in different regions worldwide. MATERIALS AND METHODS: A collaborative network task force was established during the early stage of the GP-TCM project and operated through exchanges, teleconferences and focused discussions at annual meetings. The task force involved coordinators, academics who are actively involved with R&D of Chinese herbal medicines, experts on monographic standards of Chinese materia medica, representatives from regulatory agencies, experts from industries in marketing Chinese medicines/herbal medicines and natural products. The co-ordinators took turns to chair teleconferences, led discussions on specific issues at AGM discussion sessions, at joint workshops with other work-packages such as WP1 (quality issues), WP3 (toxicology issues) and WP6 (clinical trial issues). Collectively the authors were responsible for collating discussion outcomes and updating written information. RESULTS: A global overview of regulations on herbal registration has been compiled during the three years of the consortium. The regulatory requirements for registration of herbal products in the EU and China were compared, and this is extended to other regions/countries: Africa, Australia, Brazil, Canada, Japan, Russia, South Korea, Taiwan, and the United States. A wide variation of the regulations for the categories of herbal products exists: food (functional food, novel foods, dietary food for special medical purpose, foods for particular nutritional use, food supplement); cosmetic, traditional herbal medicine products; herbal medicines for human use and veterinary use. CONCLUSION: The regulatory issues for registration of herbal products are complicated among the countries and regions worldwide. The information summarised in the text is for reference only. Some regulations which are presented in this review are still in legislation process and may change in due course. Before taking any regulatory action, readers are advised to consult current official legislation and guidance and/or to seek appropriate professional advice. The lessons learnt from global regulation of TCM will provide valuable insights for regulation of other traditional medicine such as Ayurveda and Unani medicine, as well as other forms of indigenous medicine. The WHO is well placed to co-ordinate a consultation process with the aim of putting forward suggestions for harmonisation to key regulatory agencies. SN - 1872-7573 UR - https://www.unboundmedicine.com/medline/citation/22373513/Future_development_of_global_regulations_of_Chinese_herbal_products_ L2 - https://linkinghub.elsevier.com/retrieve/pii/S0378-8741(12)00113-4 DB - PRIME DP - Unbound Medicine ER -