National Policy on Traditional Medicine and Regulation of Herbal Medicines - Report of a WHO Global Survey
(2005; 168 pages) Ver el documento en el formato PDF
Índice de contenido
Ver el documentoAcknowledgements
Ver el documentoExecutive summary
Ver el documentoAcronyms, abbreviations and definitions
Ver el documentoWHO Regions
Abrir esta carpeta y ver su contenido1. Introduction
Abrir esta carpeta y ver su contenido2. National policy on traditional medicine and complementary/alternative medicine
Cerrar esta carpeta3. The regulatory situation of herbal medicines
Ver el documento3.1 Law or regulation on herbal medicines
Ver el documento3.2 Regulatory status of herbal medicines
Ver el documento3.3 Claims
Ver el documento3.4 Pharmacopoeias
Ver el documento3.5 Monographs on herbal medicines
Ver el documento3.6 Manufacture of herbal medicines
Ver el documento3.7 Safety and herbal medicines
Ver el documento3.8 Registration system for herbal medicines
Ver el documento3.9 Herbal medicines and the essential drug list
Ver el documento3.10 Post marketing surveillance of herbal medicines
Ver el documento3.11 The sale of herbal medicines
Ver el documento3.12 Annual market sales of herbal medicines
Abrir esta carpeta y ver su contenido4. Member States, WHO and herbal medicines
Abrir esta carpeta y ver su contenido5. Country summaries
Ver el documentoReferences
Ver el documentoAnnex 1. Text of survey instrument
 

3.1 Law or regulation on herbal medicines

In the survey form, reference was made to the previous definitions of laws and regulations provided for TM/CAM. Herbal medicines have been defined above in the Introduction. In addition, in some countries, animal and mineral materials may be present in herbal medicines.

Member States were asked whether laws or regulations existed for herbal medicines; if they replied yes, follow up questions asked for the year of issue of such laws or regulations, and the type of law or regulation. The options for the type of law or regulation included the same law or regulation as for conventional pharmaceuticals, a separate law or regulation for herbal medicines, or a law or regulation partly the same as for conventional pharmaceuticals.

Survey responses indicate that a majority of responding Member States (92 countries, 65%, Figure 12) have laws or regulations on herbal medicines.


Figure 12. Laws or regulations on herbal medicines

Information provided by 77 of the responding Member States about the year of issue of the law or regulation indicates clearly that the development of laws and regulations on herbal medicine is a recent phenomenon (Figure 13). Over the last 15 years, the number of Member States with laws and regulations on herbal medicines has increased dramatically. The highest number of laws and regulations on herbal medicine were issued between 1996 and 1999.


Figure 13. Number of Member States with laws or regulations on herbal medicines, by year

Responses from those Member States having laws or regulations governing herbal medicine largely indicate that these are similar to laws or regulations on conventional medicine (see Figure 14). As responding Member States were able to choose all categories of law or regulation as required, the total number of answers in the chart below exceeds the number of respondents. As many Member States have more than one law or regulation pertaining to herbal medicines, many Member States indicated more than one category for the type of law or regulation. The total number of Member States which responded to this question was 91.


Figure 14. Type of law or regulation on herbal medicines

Finally, Map 6 below illustrates the Member States responding to the Global Survey which have laws or regulations on herbal medicines.


Map 6. Member States with law or regulation on herbal medicines

Ir a la sección anterior
Ir a la siguiente sección
 
 
El Portal de Información - Medicamentos Esenciales y Productos de Salud de la OMS fue diseñado y es mantenido por la ONG Human Info. Última actualización: le 5 noviembre 2014