Abstract
Homeopathy has a long tradition and a well-established use in Europe, especially in France, the United Kingdom, and Germany. Homeopathic medicinal products are medicinal products as defined in Article 1 of the European Council Directive 65/65 EEC and in Article 2 of the German Medicines Act (AMG). The legal and terminological framework for homeopathic medicinal products in Germany and the European Union (EU) is laid down clearly in the European Pharmacopoeia, the European Council Directives 92/73 and 92/74 EEC and, on a national level, in the German Homeopathic Pharmacopoeia (HAB1). Homeopathic products may be registered without any indication claim or they may obtain a marketing authorization allowing indication claims.Strict control of the safety of homeopathic medicinal products is necessary, because they may present risks. Therefore, homeopathic products should be included in pharmacovigilance systems. Safety requirements, however, should not be applied in a way that might discriminate against this pa...
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