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Market access for Chinese herbal medicinal products in Europe-A ten-year review of relevant products, policies, and challenges

Journal

PHYTOMEDICINE
Volume 103, Issue -, Pages -

Publisher

ELSEVIER GMBH
DOI: 10.1016/j.phymed.2022.154237

Keywords

Chinese herbal medicine; Herbal medicinal products; Traditional Chinese medicine; Registration; Market access; Europe

Funding

  1. Yunnan Quality and Technology Supervision Bureau [KKPT202126008]
  2. Yunnan Administration for Market Regulation [KKPT202026010]
  3. Key R&D Project of Yunnan Provincial Science and Technology Department [202003AC100013]
  4. Wang Mei Expert Workstation of Yunnan Province [201905AF150001]
  5. Major S&T Project of Yunnan Provincial Science and Technology Department [202102AA310048-4]
  6. Ye Zhao R&D Project of Shaanxi Province [2017ZDXM-SF-017]

Ask authors/readers for more resources

With increasing demand for natural and effective health products in Europe, the market for herbal products is growing. However, there are limited registrations of Chinese herbal medicine (CHM) products in the European Union (EU), posing challenges for pharmaceutical companies seeking market access. To successfully register CHM products, companies are advised to comply with EU regulations, consider the medication habits and pharmaceutical needs of the European market, and collaborate with local organizations in Europe.
Background: With increased consumer demand in Europe for natural and efficacious health products, the use of herbal products in the market is rising. Products of Chinese herbal medicine (CHM) could greatly expand European consumer options; however, only seven herbal medicinal products (HMPs) based on CHM formulae have been registered in the European Union (EU) since 2012. Purpose: This study reviews the ten-year registration status of HMPs based on CHM formulae in Europe and identifies major challenges and possible solutions for pharmaceutical companies seeking market access for new HMPs. Methods: An overview of relevant EU regulations identifies pathways to market access in EU countries for CHM products. A discussion of successful attempts to register HMPs based on CHM formulae since 2012 highlights specific challenges that applicants can expect to face. Results: CHM products can enter the EU market as HMPs through the full or well-established use marketing authorization, or through the simplified registration procedure. Alternatively, some CHM products have entered the market as dietary supplements, nutritional foods, and agricultural products; however, under these categories, claims for medicinal use cannot be advertised. Since the registration of the first CHM product, Diao Xin Xue Kang (with the single component of Dioscorea nipponica rhizome), in 2012, only six other HMPs based on CHM formulae have been successfully registered. Among these, four are mono-component products. The remaining two products contain combinations of several herbal ingredients. It is more difficult to register combination products than mono-component products, due to their more complex composition and differences in registration requirements (esp. concerning establishing indications) in China and Europe. Conclusions: To promote the successful registration of CHM products in Europe, pharmaceutical companies are advised to: demonstrate full control of, and the ability to test, their supply chain and manufacturing procedures following the guidance of European competent authorities; carefully adhere to all steps of the registration process and advices from European competent authorities; take the medication habits and pharmaceutical needs of European market into consideration; and establish collaboration with European local organizations, as appropriate.

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