Regulatory Situation of Herbal Medicines - A Worldwide Review
(1998; 49 pages) [French] [Spanish] Ver el documento en el formato PDF
Índice de contenido
Ver el documentoFOREWORD
Abrir esta carpeta y ver su contenidoI. INTRODUCTION
Abrir esta carpeta y ver su contenidoAfrica
Cerrar esta carpetaThe Americas
Ver el documentoAntigua and Barbuda
Ver el documentoArgentina
Ver el documentoCanada
Ver el documentoChile
Ver el documentoColombia
Ver el documentoMexico
Ver el documentoNicaragua
Ver el documentoUnited States of America
Abrir esta carpeta y ver su contenidoEastern Mediterranean
Abrir esta carpeta y ver su contenidoEurope
Abrir esta carpeta y ver su contenidoSouth East Asia
Abrir esta carpeta y ver su contenidoWestern Pacific
Ver el documentoIII. CONCLUSION
Ver el documentoIV. REFERENCES


In August 1992, the Unidad de Medicina Tradicional was established with the objective to incorporate traditional medicine with proven efficacy into health programmes, and to contribute to the establishment of their practice. A regulation for the control of the practice of alternative medicines was developed, and a legal basis was created (la Ley no. 19.253 of October 1993) which takes into consideration the role of traditional medicine in public health [20].

Legal Status

Natural products are legally differentiated as follows (Código Sanitario):

- drugs intended to cure, alleviate, or prevent diseases (article 97);
- food products for medicinal use and with therapeutic properties (article 98); and
- food products for nutritional purposes (article 108).

According to a regulation for the control of drugs, food products for medicinal use, and cosmetics (decreto no. 435/81), herbal products with therapeutic indication claims and/or dosage recommendations are considered to be drugs. Their distribution is restricted to pharmacies and drugstores which need a special authorization from the Ministry of Health. A registration for marketing authorization is needed for herbal products, homoeopathic products, and other natural products as defined in article 24 of the regulation. An application for registration consists of the complete formula, the labelling, samples of the product, and a monograph which permits identification of the formula and characteristics of the product [20].

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