TRAINING AND WORKSHOPS
Workshop Pre-Day “A strategic approach to early-stage product development” at Animal Health, Nutrition & Technology Innovation Europe by KISACO Research delivered by Argenta Global. Join us in London on 6-8 March 2023.
At this masterclass you will receive practical advice on determining the novelty of your protein, as well as find out what should be the next steps if it is novel.
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.
Virtual Seminar: The preparation of novel food dossiers in the EU under the transparency regulation. 31 May – 1 June 2022
This interactive course has been designed to give practical advice on building and submitting a novel food dossier in the EU. You will gain a comprehensive overview of the entire registration process, from notifying studies to structuring and compiling a novel food dossier, the submission process and how to comply with the latest changes following the Transparency Regulation.
This course has been designed to give practical advice and guidance on how tocompile an EU-compliant food supplement label, ensuring you gain a comprehensive insight into the legal framework, necessary requirements and permitted claims, as well as providing tips and links to key resources.
This course has been designed to give practical advice and guidance on how to compile an EU-compliant feed and feed additive label, ensuring you gain a comprehensive insight into the legal framework, necessary requirements and permitted claims, as well as providing tips and links to key resources.
Practical Course: A Regulatory Update on Animal Feed and Feed Additives in the EU (European Union) and USA. 2-3 December 2021
Pen & Tec Consulting, together with Management Forum, will deliver this practical and interactive two-day course that 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).
Virtual Seminar: A Post-Transparency Guide to Feed Additive Registration in the EU. 15-16 November 2021
This interactive course has been designed to give practical advice on building and submitting a feed additive dossier in the EU. You will gain a comprehensive overview of the entire registration process, from notifying studies to structuring and compiling a feed additive/renewal dossier, the submission process and how to comply with the latest changes following the Transparency Regulation.
This course will take participants through all of the necessary steps to obtain marketing authorisation for a feed additive in the European Union.
IP & data protection for alternative proteins: how to protect your products in the EU – joint webinar by BGP, HGF & Pen & Tec Consulting
Join us for our free webinar which will highlight what you can do to protect your alternative protein product, what are the data requirements for a patent & how long does it take and other topics.
Webinar with Dr Eliana Henriquez-Rodriguez: “Transparency Regulation and the EU food and feed industry – latest updates”
During this short webinar, we will share the latest updates provided by European authorities regarding the key points that will affect applications for requesting authorisations for food and feed products in the EU – notification of studies to the new EFSA database, public consultations, as well as dossier preparation and submission.
FREE LIVE Webinar with Rosalia Flores: “Traditional Food from third countries: regulatory landscape and procedure for the EU market”
Traditional foods from third countries are a special kind of novel foods & have a simplified authorisation process & dataset. This Webinar will provide an overview of the regulatory landscape and procedure to introduce your traditional food on the EU market. We will go through the data required to prepare a successful dossier, explore the notifications submitted to date and highlight the main safety concerns raised by the authorities.
“Cannabis derived products in novel foods & cosmetics. How to get them to the market?” – joint webinar with Ayton Global Research & Aurora Hemp
Having issues trying to make sense of the regulatory landscape for CBD and Cannabis derived products? How to get them to the market and ensure they stand out against competition? Let us simplify things for you!
This webinar will provide an overview of the Biocidal Products Regulation and the approval routes for biocidal active substances & biocidal products in the EU, focusing on the simplified authorisation procedure, and will examine the bridges between the registration procedures for biocides and feed additives.
This webinar will cover the main changes introduced after the implementation of Regulations 2016/127 and 2016/128. We will analyse the legal situation of some trend ingredients (protein hydrolysates, probiotics and human oligosaccharides) and how these are intertwined with Novel Food Regulations and other EU provisions.
Webinar with Laura Payo Lewis: EFSA regulatory requirements for EU approval of microbial feed additives
Microorganisms are widely used in the food chain as such or as production organisms of products of interest. The placement of such microorganisms, genetically modified or not, or derived substances in the European market may be subject to a pre-market authorisation process, which involves a risk assessment by the European Food Safety Authority. If you would like to learn about the regulatory requirements to characterise micro-organisms, including Whole Genome Sequence analysis, don’t miss our free webinar!
Webinar with Dr Eliana Henriquez Rodriguez: EFSA Study design tips & tricks for feed additive efficacy & target animal safety studies
This webinar will cover the study design requirements that are detailed on EFSA guidelines and those that are not, as well as specific advice for handling data, performing statistical analyses, and preparing a final EFSA compliant study report. We will also share with you our tips & tricks, obtained during our almost 20 years of experience with feed additive applications, for avoiding the common pitfalls that applicants encounter during the EFSA evaluation procedure.
Plant based meat replacers are already available on the EU market and welcomed by consumers. Other novel protein sources are being developed and often produced by emerging technologies. R&D departments are working hard on making the production process cost effective for the consumer and as sustainable as possible, but is there anything else they should be taking into account at this stage? If you want to learn the answers to these or related questions, then tune in to our free webinar!
FREE Webinar with Nicoleta Pasecinic: EU novel food updates: Two years on – has the new novel food regulation made it easier for applicants?
In January of 2018 the new Regulation on novel food entered into force. Almost 2 years after, we can learn how strict has been EFSA Panel on Nutrition, Novel Foods and Food Allergens (NDA) at assessing the novel food applications that came through. If you want to get up to date with the current state of play of the EU novel food applications, then tune in to our free webinar!