Date: On-demand - This is a recording of the live webinar which took place in August 2018.
This webinar is a quick, but comprehensive overview of the current status of feed additive efficacy, as evaluated by EFSA, as well as an indicator of future opportunities for EU-approved feed additives. The webinar covers the requirements for an EU feed additive efficacy data set, within the current EU/EFSA framework for authorisation of feed additives.
- The EU regulatory framework – relevant legislation
- Types of feed additives and acceptable claims
- Data requirements – product characterization safety, quality and efficacy
- Applicable guidelines and guidance documents (EC, EFSA and EURL)
All target audiences are applicable, from beginners to experienced regulatory professionals, since the EFSA 2018 feed additive guidance document is new & enters into force on 1 September 2018. This TOPRA Webinar explains the background & legal framework of the new EFSA guidance. Due to the EU feed additive REFIT programme, currently underway, there are opportunities to influence future EU & EFSA approaches to the requirements to demonstrate feed additive efficacy and related permissible claims. The course may be of interest to CROs offering in vitro, ex vivo or in vivo testing facilities, as well as global stakeholders such as non-EU regulatory authorities.
Dr Elinor McCartney, President, Pen & Tec Consulting Group
Dr Elinor McCartney has over 30 years’ experience in product development and EU regulatory affairs for multiple categories, including food and feed additives, novel foods and nutrition and health claims. Elinor is a graduate of the Royal (Dick) School of Veterinary Studies, University of Edinburgh, where she also obtained a PhD in enteric diseases of piglets. She has an MBA (with distinction) and has tutored Finance and Marketing for the Open University Business School.
In 2000, Elinor set up Pen & Tec Consulting to help companies comply with EU regulations and legally sell their food and feed products in Europe. Elinor mainly provides strategic advice to clients on legal status and best regulatory options to accelerate time to market. Elinor is a frequent and popular speaker at international conferences on topics such as probiotics and nutritional support for human and animal health, and is also the author or co-author of over 25 manuscripts published in peer-reviewed scientific journals
This course offers 1 CPD hour for successful completion, to learn about why CPD is important visit the Lifelong Learning page.
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