herbal medicine schools

The Traditional herbal medicines more safety for products put on European market - Herbal Products, Herbal Directive, Herbal Market, UE Herbal Market,  herbal medicinal product ; Brussels. From tomorrow, EU citizens can be reassured that the traditional herbal medicines they buy in the EU are safe and effective, the EU Representation in Sofia announced. The expiry of the 7 year transition period set out in the 2004 Herbal Directive (2004/24/EC) means that only medicinal products which have been registered or authorised can remain on the EU market after 1 May 2011.

The Herbal Directive introduces a simpler registration procedure than for other medicinal products, in respect of the long history of use of traditional herbal medicinal products. At the same time, the Directive provides the necessary guarantees of their quality, safety and efficacy.

John Dalli, European Commissioner for Health and Consumer Policy, said, "We have now reached the end of a long transition period which has given producers and importers of traditional herbal medicinal products the necessary time to show that their products have an acceptable level of safety and efficacy. Patients can now be confident about the traditional herbal medicinal products they buy in the EU."

In order to protect public health, all medicinal products, including traditional herbal medicinal products, need a marketing authorisation to be placed on the EU market. The simplified procedure introduced by the Herbal Directive allows these products to be registered without the safety tests and clinical trials that a full marketing authorisation procedure would involve.

Instead, an applicant who wishes to register a traditional herbal medicinal product must provide documentation showing that the product in question is not harmful in the specified conditions of use. They must also provide evidence that the product has a proven track record, ie. that it has been used safely for at least 30 years – 15 of these in the EU.

The Herbal Directive was adopted by the European Parliament and the Council on 31 March 2004. It gave an exceptionally long transition period of 7 years for manufacturers to register their traditional herbal products already on the EU market when the Directive entered into force.

Applicants have had 7 years to apply to the competent authority in the Member States(s) where they wanted to market their product. If, by 30 April 2011, a herbal medicinal product is not registered or authorised, then it may not be on the EU market after 1 May 2011. After this date, producers of traditional herbal medicines can still apply for a registration through the simplified registration procedure.

Does not ban traditional medicines from the European market. On the contrary, it introduces a lighter, simpler and less costly registration procedure than for other medicinal products. Plus it has given producers of traditional herbal medicinal products an exceptionally long transition period of 7 years to register their products.

Does not ban vitamins, mineral supplements and herbal teas.

Does not ban alternative therapies and therapists, homeopathy, plants or books on plants. Source http://www.focus-fen.net/index.php?id=n248329