Regulatory Situation of Herbal Medicines - A Worldwide Review
(1998; 49 pages) [French] [Spanish] View the PDF document
Table of Contents
View the documentACKNOWLEDGEMENTS
View the documentFOREWORD
Open this folder and view contentsI. INTRODUCTION
Close this folderII. REGULATORY SITUATION
Open this folder and view contentsAfrica
Open this folder and view contentsThe Americas
Open this folder and view contentsEastern Mediterranean
Close this folderEurope
View the documentGeneral aspects
View the documentAttempts to Meet the Need for Harmonization
View the documentAustria
View the documentBelgium
View the documentBulgaria
View the documentDenmark
View the documentEstonia
View the documentFinland
View the documentFrance
View the documentGermany
View the documentGreece
View the documentHungary
View the documentIceland
View the documentIreland
View the documentItaly
View the documentNetherlands
View the documentNorway
View the documentPortugal
View the documentSpain
View the documentSweden
View the documentSwitzerland
View the documentTurkey
View the documentUnited Kingdom
Open this folder and view contentsSouth East Asia
Open this folder and view contentsWestern Pacific
View the documentIII. CONCLUSION
View the documentIV. REFERENCES
 

Denmark

Under the Danish Ministry of Health Order No. 790 of 21 September 1992 [47], natural remedies covered by the authorization system are defined as follows:

- Natural remedies shall be understood to mean medicinal products in which the active substance (content) exclusively comprises naturally occurring substances in concentrations that are not substantially greater than those in which they are found in nature.

- The order applies to natural remedies intended for oral use or application on skin or mucous membranes. It does not apply to remedies containing prescription-only drugs, nor to homoeopathic medicines.

Combinations of natural remedies with added vitamins and/or minerals cannot be marketed as natural remedies. Proof of quality, safety and efficacy must be given; a bibliographic application with respect to therapeutic use is accepted if it contains descriptions in the relevant scientific literature of Europe or North America [47,48].

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