This seminar has been designed to give a practical overview on how to register a feed additive in the EU. You will learn how the registration process works, including the latest changes that apply after the implementation of the Transparency Regulation. Additionally, the presenters will also discuss several pioneer applications evaluated by EFSA as well as borderline cases between feed additives and veterinary medicines.

• Understand the feed additive registration process
• Learn what is the content of a feed additive dossier
• Gain a practical insight into how to comply with the Transparency Regulation
• Learn relevant aspects of the risk assessment provided for pioneer products

Dr Eliana Henriquez Rodriguez

Eliana is an agricultural engineer with a PhD in agricultural and food science and technology. She has a strong scientific background, developing skills in animal production management, molecular genetic techniques, statistical analysis and scientific writing.  

As well as being an experienced regulatory project manager and public speaker, Eliana is Pen & Tec’s Transparency Regulation expert. She provides internal and external training on the registration process of feed and feed additives, EFSA-compliant studies and the latest changes under the new Transparency Regulation. 

Laura Payo Lewis

Laura is a biotechnologist with over 10 years’ regulatory experience related to food and feed product registrations in the EU and worldwide. Laura regularly delivers seminars on the registration process for feed and feed additives in the EU and other countries.

She is also experienced in designing client and in-house training sessions covering all aspects of the EU registration process, on topics such as understanding data requirements for the risk assessment of novel food and feed products, avoiding questions from the authorities and providing strategic registration options.

Dr. Cornelia Hüttinger

Head of Regulatory Affairs at Klifovet 

From 2018 onwards, Cornelia has acted as scientific group leader regulatory affairs with specific focus on biological products

Since December 2020 she is heading the Regulatory Affairs Department at Klifovet where she is responsible for general strategic regulatory advice, registration and regulatory life cycle activities of feed, feed additives incl. microbiome products, non-biological and biological veterinary medicinal products.

To book the course please follow the link.