As a result of the EU White Paper on Food Safety published in 2000, there have been sweeping changes to legislation concerning the food chain, especially feed and feed additives. The EU feed additive regulation (EC No. 1831/2003) replaced the existing feed additive Directive 70/524/EEC and introduced a new system for assessing feed additive dossiers. The new evaluation procedure involves the EU Commission, EFSA (European Food Safety Authority) and the Standing Committee on the Food Chain and Animal Health, which includes delegations from 25 EU Member States. The EU plans to review all currently authorised feed additives within the next decade, most likely starting with groups of additives that are considered to represent a potential safety hazard to animals, workers, consumers or the environment. Many existing feed additives have never before been subjected to an EU assessment according to current standards of safety, quality and efficacy.
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Weblink: http://www.management-forum.co.uk/html/con_semin_section/con_display_event.asp?id=504
- Name des EventsRegulatory Update On Animal Feed Additives
- Adresse der VeranstaltungThe Rembrandt Hotel
- Stadt/RegionLondon
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Management Forum organise Conferences and Seminars on specialised topics relating to aspects of Biotechnology, Complementary Medicine, General Healthcare, Human Resources, Intellectual Property, Medical Devices, Nutritional Sciences, Pharmaceutical and Veterinary Medicine.
Our events cover a variety of areas including: production manufacturing, regulatory affairs, pharmacovigilance, clinical trials, research and development, therapeutics, respiratory medicine, marketing, health economics, quality assurance, patents and trade marks and licensing.
Attendance at Seminars is usually limited in order to offer ample opportunity for informal discussion. We also organise international Conferences on important issues affecting the pharmaceutical and related industries.
Our events cover a variety of areas including: production manufacturing, regulatory affairs, pharmacovigilance, clinical trials, research and development, therapeutics, respiratory medicine, marketing, health economics, quality assurance, patents and trade marks and licensing.
Attendance at Seminars is usually limited in order to offer ample opportunity for informal discussion. We also organise international Conferences on important issues affecting the pharmaceutical and related industries.