Free Webinar: “Early-stage product development: the cost of having your regulatory strategy right”
16 February 2023, 3 PM CET, On-line
In the EU, feed additives are products used in animal nutrition which are intentionally added to feed or water in to favourably affect the quality of feed and the quality of food from animal origin, or to improve the animals’ performance and health. Feed additives must undergo a pre-market safety assessment via a centralised before being placed on the EU market. The scientific safety assessment is carried out by the European Food Safety Authority (EFSA) and the authorisation of the additive is granted by the European Commission (EC).
Since March 2021, Regulation (EU) 2019/1381 on transparency has applied to all regulated products in the food chain. Now all studies used to support an application must be notified to EFSA prior to the study start, and some will require co-notification. Confidential data must be fully justified by the applicant, and a non-confidential version of the dossier will be made publicly available.
Join this webinar to get a perspective on the registration process of a feed additive in the EU and to understand the importance of getting the regulatory strategy right from the start. You will learn how the registration process works, how to avoid common mistakes, reduce costs and speed up time to market.
Duration: 30 min presentation + 10 min Q&A session.
- Project managers
- Regulatory managers
- Scientists that are interested in finding out more about this complex process and how to comply with the latest changes and challenges following the transparency regulation
Laura Payo Lewis
Regulatory Affairs Director
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.
To book the webinar please follow the link.
If you are interested in learning more about the development and registration strategy not only for feed products, but also for veterinary medicinal products or medical devices, please be sure not to miss the workshop delivered by Argenta Global at KISACO Research in London on the 6-8 March. Register here to attend the event and to learn all about planning studies and regulatory requirements in EU & US markets through innovative and real practical examples.