Presented by
Management Forum
Annual two-day regulatory update on animal feed and feed additives in the EU, USA and China.
★★★★★ "Great webinar, very useful, excellent speakers. Content was interesting, plenty new information, use... more (32)"
2-3 December 2024 »
from £1299.00
Meeting regulatory requirements for feed and feed additives in the EU and other key markets such as China and the USA are major challenges for businesses in the field of animal nutrition. In this, two-day course, split over two half-days, you will hear the latest requirements from both the Food Standards Agency (FSA) and the EFSA (European Food Safety Authority) and you from key personnel from knoell China and Argenta US and EU.
This course forms part of our selection of Animal Health training courses, designed to keep you up to date with the latest regulations surrounding veterinary medicines, animal feeds, and industry best practices.
Dr Jaume Galobart is a veterinarian with a PhD in Animal nutrition. He is currently a Senior Scientific Officer in the FEEDCO unit of the European Food Safety Authority. He has over 20 years experience in the assessment of feed additives and the development of guidance documents. He is the coordinator of the FEEDAP Panel of EFSA, where he has also coordinated many of its working groups.
Bo Yang, Managing Director of Knoell Shanghai, has been working at knoell in the regulatory consulting field for 10 years. Through these years’ development, Knoell Shanghai has build up a strong expert team and experience on pre-market approval process for feed and feed additive products. As a part of Knoell global group, the local team is well-equipped to assist the global manufacturers and trading companies to bring their imported products into the Chinese market.
Bi Jun is a pharmaceutical expert with more than 10 years of experience in health product development and registration in China. Currently in Knoell Shanghai, he is mainly responsible for regulatory support and the registration of pharmaceutical ingredients and packaging materials for human drugs (DMF), Biocides, feed/feed additives and veterinary drugs.
Heather Sedlacek is the Regulatory Affairs Manager at Argenta Kansas, bringing over 20 years of experience in the animal drug industry. She is a veterinarian with a master’s degree in veterinary biomedical science and a graduate certificate in Animal Health Regulatory Affairs. Heather specializes in strategic regulatory guidance for both pre-approval and post-approval stages of animal drugs, including pioneer and generic drugs, as well as animal feeds. She also serves as the Regulatory Affairs Advocate and Legislative Action Subgroup Chair for the Generic Animal Drug Alliance (GADA) and is the Alternate Affiliate Representative to the Animal Health Institute (AHI) Veterinary Biologics Section Steering Committee.
Dr. Andrew Bell is dedicated to ensuring regulatory excellence and compliance, leveraging his scientific expertise to effectively navigate the complex regulatory landscape. He has a solid background in regulatory affairs and a decade of experience in analytical microbiology. Andrew’s experience is supported by a PhD in Microbiology, which laid the foundation for his success in both analytical and regulatory disciplines. He brings a wealth of knowledge to the feed additives and novel food industries, supporting clients in their feed additive applications from project inception through study design, dossier submission, and EU authorisation.
NEW higher discounts for multiple bookings - bring your colleagues to make your training budget go further:
Please contact us for pricing if you are interested in booking 5 or more delegates
2-3 December 2024
Live online
12:30-16:30 UK (London) (UTC+00)
13:30-17:30 Paris (UTC+01)
07:30-11:30 New York (UTC-05)
Timings may be different for each day
Course code 14080
Limited places remaining
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* Early booking discounts may not be combined with other discounts or offers. As such, the discounts for 2nd/3rd/4th delegates are based on the full price; and apply only when booking multiple delegates on the same date.
Great webinar, very useful, excellent speakers. Content was interesting, plenty new information, useful guidelines and practical advice.
Dec 4 2023
Ksenija Buncic
Regulatory affairs assistant, PATENT CO.COM
Dec 4 2023
I really appreciate the professionality and the experience of speakers and the good summary in the presentations.
Elisa Fochi
Quality Assurance and Regulatory Manager, Vetagro SpA
Dec 4 2023
Very informative, good speakers
Natallia Serwatka
Head of Export Compliance, Mervue Laboratories
Dec 4 2023
The presentations were clear, precise, and enriched with numerous real-life examples and case studies illustrating the intricacies of navigating complex registration processes. Overall, the course was excellent.
Benedit Leo Kristain Jayaseelan
Regulatory affairs & Quality technician , Symrise Aqua Feed
Dec 2 2021
Very clear and comprehensive presentations.
Kalinka Grozeva
Quality Control Director, Vetagro S.p.A.
Dec 2 2021
Much more information was provided than I expected, it was VERY useful and well prepared.
Annette Spielbauer
Inoculant Registration and QC Associate, CORTEVA
Dec 2 2021
Excellent content. Knowledgeable experienced speakers. Lots of practical examples.
David Pickard
Regulatory Manager, Inroads International Ltd
Dec 2 2021
Very good: professional & very relevant. Also the many examples given by Elinor were really interesting
Isabelle Lardon
Regulatory affairs Coordinator, INVE
Dec 2 2021
during the seminar it was very clear that all speakers have a lot of experience in their fields and I liked the examples, to better understand the process and the time lines
Melanie Wergin
Medical Research Manager, Biologisce Heilmittel Heel GmbH
Dec 5 2019
Excellent course content with very useful and topical discussions. The speakers were competent and captivating with a good presentation pace.
Kalinka Grozeva
Quality Control Director, Vetagro S.p.A.
Dec 5 2019
Well-organised course with the relevant content I needed to stay on top of the field and a good opportunity to meet other professionals. I very much appreciated having the printed presentations as it makes taking notes much more efficient.
Adalberto Costessi
Product Manager, BaseClear
Dec 5 2019
All speakers delivered their presentations in a clear and concise manner, supported by informative slides.
Beccy Christmas
Regulatory Affairs Officer, Micron Bio-Systems Ltd
Dec 5 2019
Very well presented, very informative content and a friendly atmosphere.
Maria Brogan
Formulation & Compliance Manager, Inform Nutrition
Dec 5 2019
As with previous years the course was very informative and gave a rounded set of opinions from various perspectives (industry, EFSA, consultants etc).
Joshua Forster
Regulatory Executive, CYTON BIOSCIENCES LTD
Dec 5 2019
Hector's presentation was the clearest analysis I have seen on the effects of Brexit on UK industry and the economy.
David Pickard
Regulatory Manager, Inroads International Ltd
Dec 5 2019
All good and informative.
Helena Oliveira
Regulatory Affairs Manager, Nutreco Nederland BV
Dec 6 2018
I think that the speakers were really very good and made an interesting meeting out of potentially dry material. Level of discussion was good. Excellent course.
Colin Capner
Project Coordinator, Ridgeway Research Ltd
Dec 6 2018
All presentations were of high quality and explained the topics covered very well.
Angelo Lauwaerts
Business Development Manager , Proviron Industries NV
Dec 6 2018
Good speakers, good program, quite general overview.
Kalinka Grozeva
Quality Control Director, Vetagro S.p.A.
Dec 6 2018
Very good content and organisation, very qualified and experienced speakers.
Juliane Dohms
International Manager Regulatory Affairs, Phytobiotics Futterzusatzstoffe GmbH
Dec 6 2018
A really nice atmosphere, very good speaker and interesting workshops.
Cornelia Hüttinger
Regulatory Affairs Manager, Klifovet AG
Dec 6 2018
Very good quality, I would recommend to new comers in this area together with also more experienced people.
Anne Cadoux
Head of Regulatory Affairs , Boehringer Ingelheim
Dec 7 2017
I really enjoyed it, the venue was good, the organizers were helpful, even the hotel staff was helpful.
Nisha Kaushik
Regulatory Affairs , Vitalus Nutrition Inc.
Dec 7 2017
Very interesting to see the updates and the speakers' opinions.
Luisa Paches Samblas
Regulatory Procedures Team Leader, Cyton Biosciences Ltd.
Dec 7 2017
I think it was excellent.
David Adimpong
Scientist & Laboratory Manager, Envirosystems.co.uk
Dec 7 2017
A very informative course, good content without being overwhelming. Clear and engaging speakers. Very comfortable surroundings.
Sarah Norton
Senior Scientific Officer, Veterinary Medicines Directorate
Dec 7 2017
Content was really great, not too heavy. All speakers were very clear and happy to take questions.
Sarah Harrison
Research Coordinator, Ridgeway Research Ltd
Dec 7 2017
A comprehensive course with clear and engaging speakers, and useful workshops.
Sarah Norton
Senior Scientific Officer, Veterinary Medicines Directorate
Dec 7 2017
Presentations, speakers and content were very comprehensive.
Dhiraj Lakhichand Jain
Proprietor, BioBota Consulting
Dec 7 2017
It was great, very global, so not only EU restricted, covered the main relevant areas in my opinion and was very well organized and carried out.
Odile Bideau
Project Manager, Chef du Monde S.L.
Dec 8 2016
Practical and pertinent.
Dora Rodriguez
Jefo Nutrition Inc
Dec 8 2016
Everything was very good.
Irene Margüenda
Regulatory Affairs Manager, Norel S.A.
United Kingdom
Germany
France
Netherlands
Belgium
Spain
Ireland
Denmark
United States of America
Finland
Austria
Italy
Switzerland
Canada
Sweden
Australia
China
Estonia
India
Israel
Poland
Portugal
Saudi Arabia
Serbia
1 day
Typical duration
Pricing from:
We can customise this course to your requirements and deliver it on an in-house basis for any number of your staff or colleagues.
Contact our in-house training experts Aleksandra Beer and Yesim Nurko to discuss your requirements:
Multiple colleagues? See above for details of our discounts for 2, 3, or 4 delegates. For more, talk to one of our training experts to discuss how to: