A Regulatory Update on Animal Feed and Feed Additives in the EU, USA and China: 2-Day Conference (London, United Kingdom - December 5-6, 2019) - ResearchAndMarkets.com

December 7, 2018

DUBLIN--(BUSINESS WIRE)--Dec 7, 2018--The “A Regulatory Update on Animal Feed and Feed Additives in the EU, USA and China” conference has been added to ResearchAndMarkets.com’s offering.

This conference will review EU legislation, examine procedures and data requirements, and discuss to what extent EFSA-compliant data can be used to achieve approvals in China and the USA (or vice versa).

Re-evaluation by the EU of around 500 feed additives started in 2010 and the EU is systematically prohibiting feed additives for which no re-evaluation dossier was submitted, or which fail the European Food Safety Authority’s (EFSA) scrutiny.

A new feed regulation, the feed material register and the catalogue of feed materials have improved transparency in feed labelling, while allowing some physiological and functional claims.

Depending on intended use, the US FDA may regulate a product added to animal feed as either a drug or a feed ingredient. In either case, the Food Drug and Cosmetic Act requires the sponsor to obtain FDA approval or GRAS recognition prior to marketing.

In the past, FDA has followed a policy of enforcement discretion to allow marketing of unapproved products if evaluated by the AAFCO feed ingredient definition process and listed in the Official Publication. The FDA now encourages sponsors to use the food additive petition procedure for new products.

The Chinese Ministry of Agriculture introduced new guidance and legislation on feed additives, adopting some aspects of EU/EFSA, other aspects of USA FDA, and some uniquely Chinese approaches in the area of animal nutrition.

For these reasons many companies manufacturing or marketing feed additives wish to address, as far as possible, the regulatory requirements of EU, Chinese and US authorities in a single project. As part of this conference, informal workshops will enable delegates to work together to solve regulatory problems.


Welcome and introduction Implementation of Regulation (EC) No 1831/2003 on Additives for Use in Animal Nutrition - An update The Role of the EU and Comitology New approaches to the risk assessment of feed additives of botanical origin - How to deal with complex mixtures and their variability? Workshop one - Strategic options for animal nutrition products in the EU Workshop feedback and discussion Networking drinks reception Review of day one - Focus on EU/EFSA - BREXIT update BREXIT Blues - Food chain blocked, broken or better? Study design and statistics - What EFSA wants The US FDA approach to the regulation of feed ingredients The Chinese approach to feed additives Workshop two - Study design and statistics Led by Dr Eliana Henriquez Rodriguez, Pen & Tec Workshop feedback and discussion Workshop three - Managing dossier projects - best practices Workshop feedback and discussion Discussion, questions and answers Close of forum

For more information about this conference visit https://www.researchandmarkets.com/research/vlhz4q/a_regulatory?w=4

View source version on businesswire.com:https://www.businesswire.com/news/home/20181207005510/en/

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Related Topics:Animal Feedstuffs



SOURCE: Research and Markets

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PUB: 12/07/2018 02:55 PM/DISC: 12/07/2018 02:55 PM


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