The European Directive on Traditional Herbal Medicinal Products (THMPD), formally the Directive 2004/24/EC amending, as regards traditional herbal medicinal products, Directive 2001/83/EC on the Community code relating to medicinal products for human use, was established by the European Parliament and Council on 31 March 2004 to provide a simplified regulatory approval process for traditional herbal medicines in the European Union (EU). Previously, there was no formal EU wide authorisation procedure, so each EU member state regulated these types of products at the national level.
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| - European Directive on Traditional Herbal Medicinal Products (en)
- 伝統生薬製剤の欧州指令 (ja)
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| - 伝統生薬製剤の欧州指令(European Directive on Traditional Herbal Medicinal Products : THMPD、正式にはDirective 2004/24/EC amending, as regards traditional herbal medicinal products, on the Community code relating to medicinal products for human use）であり、欧州連合(EU)における、伝統的な植物薬のための簡便な規制承認手続きとして、2004年3月31日に、欧州議会および同理事会によって定められた。以前にはEU全体にわたる公式な承認方法はなかったので、それぞれのEU加盟国は、国としてこうした製品を規制していた。この規制の下では、すべての生薬製剤はEU内での販売許可を取得する必要がある。 薬草医の指導を受け患者のためにつくられる承認されていない治療薬は、伝統生薬製剤の指令の条件から除外される。 生薬製剤は、完成品の質の確保と、また安全性を示すために(GMP)に従って製造される。 (ja)
- The European Directive on Traditional Herbal Medicinal Products (THMPD), formally the Directive 2004/24/EC amending, as regards traditional herbal medicinal products, Directive 2001/83/EC on the Community code relating to medicinal products for human use, was established by the European Parliament and Council on 31 March 2004 to provide a simplified regulatory approval process for traditional herbal medicines in the European Union (EU). Previously, there was no formal EU wide authorisation procedure, so each EU member state regulated these types of products at the national level. (en)
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| - Directive on Traditional Herbal Medicinal Products (en)
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| - The European Directive on Traditional Herbal Medicinal Products (THMPD), formally the Directive 2004/24/EC amending, as regards traditional herbal medicinal products, Directive 2001/83/EC on the Community code relating to medicinal products for human use, was established by the European Parliament and Council on 31 March 2004 to provide a simplified regulatory approval process for traditional herbal medicines in the European Union (EU). Previously, there was no formal EU wide authorisation procedure, so each EU member state regulated these types of products at the national level. Under this regulation, all herbal medicinal products are required to obtain an authorisation to market within the EU. Those products marketed before this legislation came into force can continue to market their product until 30 April 2011, under the transitional measures defined in the Traditional Herbal Medicinal Products Directive. Once this time limit has expired, all herbal medicinal products must have prior authorisation before they can be marketed in the EU. For those herbal medicinal products that were not on the market before 30 April 2004, an authorisation must be obtained prior to marketing. The only herbal medicines that are exempted from the provisions of the Traditional Herbal Medicinal Products Directive are those unlicensed remedies that are made up for a patient following a consultation with a herbalist. Herbal medicines must be now manufactured under Good Manufacturing Practice (GMP) to ensure the quality of the finished product and also demonstrate safety. Under the Traditional Herbal Medicinal Products Directive, a company needs to demonstrate that the herbal medicine has been in use within the EU for at least 30 years or 15 years within the EU and 30 years outside the EU. There is concern that some herbal remedies of 30 years ago, which are no longer in widespread use, could still be sold but that valid new herbs which cannot meet the 30-year rule may require to be withdrawn from sale. The rule could also mean that it may not be possible to license some traditional herbal medicines which were in common use more than 30 years ago, but have since fallen into disuse. There are key eligibility criteria for a herbal medicine to qualify under this legislation:
* Only herbal medicines that are administered orally, externally, or by inhalation are suitable. Any medication that requires intravenous administration will not be authorised.
* Only herbal medicines that are intended to be used without supervision by a medical doctor will be authorised by this scheme.
* The intended use of a herbal medicine will only be authorised on the basis of its traditional history and/or the recognised pharmacological properties of the herbal ingredient(s).
* Vitamins and minerals may be added to the herbal medicine provided that their use is ancillary to the herbal ingredient(s).
* If the competent EU member judges that the herbal medicine fulfills the criteria for a marketing authorisation, then an authorisation under Traditional Herbal Medicines Product Directive should be granted.
* Herbal medicine products manufactured using isolated active ingredients from plants will not be regarded as herbal medicines and will not receive an authorisation under this scheme. The Traditional Herbal Medicines Product Directive does allow medicinal claims to be made on the label of the final product, although restrictions do apply on the final wording. (en)
- 伝統生薬製剤の欧州指令(European Directive on Traditional Herbal Medicinal Products : THMPD、正式にはDirective 2004/24/EC amending, as regards traditional herbal medicinal products, on the Community code relating to medicinal products for human use）であり、欧州連合(EU)における、伝統的な植物薬のための簡便な規制承認手続きとして、2004年3月31日に、欧州議会および同理事会によって定められた。以前にはEU全体にわたる公式な承認方法はなかったので、それぞれのEU加盟国は、国としてこうした製品を規制していた。この規制の下では、すべての生薬製剤はEU内での販売許可を取得する必要がある。 薬草医の指導を受け患者のためにつくられる承認されていない治療薬は、伝統生薬製剤の指令の条件から除外される。 生薬製剤は、完成品の質の確保と、また安全性を示すために(GMP)に従って製造される。 (ja)
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