Stay ahead: Explore OECD, EFSA & ECHA guidance, tools, and best practices for applying read-across in toxicology and chemical risk assessment. This conference meets diverse industry needs. Join experts, regulators & peers to expand knowledge, share case studies, and prepare for future challenges.
With increasing demands for reliable, scientifically robust alternative methods, read-across has become an essential tool for regulatory toxicology and chemical risk assessment in various industries – but practical implementation remains challenging. The conference will bring together top-tier experts, regulators, and industry practitioners to share the latest guidance, practical workflows, and best practice examples for read-across approaches.
This conference is designed for professionals working in toxicology, human risk assessment, registration and regulatory affairs, R&D, product stewardship & responsible care and human & consumer safety across the chemical, biocide, agrochemical, cosmetic, food and feed industries, research institutes, regulatory authorities, testing laboratories and professional associations.
Regulatory framework and developments
Tools and harmonised workflows
Advanced methods and case studies
Professionals working in the fields of:
Sectors that should take part:
Picture Credit: © apinan – AdobeStock
We are currently in the process of compiling our event programme in close cooperation with our team of experienced speakers.
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Name
Company
Arianna Bassan
Innovatune, Italy
Arianna Bassan is a consultant and European Registered Toxicologist (ERT) with a multidisciplinary background in chemistry, biology, and toxicology. As co-founder of Innovatune, she specializes in human health hazard assessment integrating (Q)SAR, read-across, and computational methods. She has led international groups on in silico toxicology and is now extending this work to AI-based toxicological risk assessment. She is the author of numerous peer-reviewed publications and reports.
morelessSusanne Hougaard Bennekou
Danish Patient Safety Authority, Denmark
Susanne Hougaard Bennekou has been a Chief Advisor at the Danish Patient Safety Authority since last year. She has worked in the Division of Risk Assessment and Nutrition at the National Food Institute of the Technical University of Denmark (DTU) as a Senior Advisor in toxicology since 2019. Previously she was a Senior Advisor in the Pesticide Division of the Danish EPA. She was the Vice-Chair of the EFSA PPR Panel, a Vice-Chair of the EFSA Scientific Committee and since 2024 she has been the Chair of the EFSA Scientific Committee.
morelessMark Cronin
Liverpool John Moores University, UK
Steven J. Enoch
Liverpool John Moores University, UK
Steven J. Enoch is a Reader in Computational Toxicology at the School of Pharmacy and Biomolecular Sciences of the Faculty of Science at the Liverpool John Moores University and has over 15 years’ worth of experience in the field of predictive toxicology. He is an expert in the use of chemical and metabolism information to predict toxicological hazard without the use of animals, especially in the development and application of computational profiling schemes for chemical category formation and read-across.
morelessSylvia Escher
Fraunhofer Institute for Toxicology and Experimental Medicine (ITEM), Germany
Sylvia Escher is a Chemist and trained Toxicologist and the Head of the Department of In-silico Toxicology at the Fraunhofer Institute for Toxicology and Experimental Medicine (ITEM). The focus of her work the use of alternative methods such as QSAR models and grouping approaches in safety and risk assessment. This include the development and maintenance of toxicological databases. For some years now, the integration of new methods in human risk assessment, such as those developed in the EUTOXRISK and EXITOX project, has increasingly become the focus of their work. In this context ITEM is developing workflows to integrate omic data as well as PBK models, specialized on uptake and distribution of airborne compounds.
morelessMonika Kemény
BASF, Germany
Monika Kemény is a Certified Toxicologist and has been a Regulatory Toxicologist at BASF, Germany, since 2006. Before joining BASF she has worked for the DFG Senate Commission on Food Safety (SKLM) since 2002.
morelessCathy C. Lester
Procter & Gamble, USA
Juan Parra Morte
European Food Safety Authority (EFSA), Italy
Juan Parra Morte has been Toxicologist in the Pesticide Peer Review Unit of EFSA since 2008. He has been actively involved in the assessment of pesticide active substances, their metabolites and impurities, including the EFSA PPR, the OECD Guidance on Residue Definition and EFSA's outsourced projects on the Genotoxicity Database and QSAR and Read-Across for the genotoxicity of metabolites. He is chairing the EFSA Working Group on NAMs QSARs.
morelessAndrea Richarz
European Chemicals Agency (ECHA), Finland
Martin Wilks
University of Basel, Switzerland
Martin Wilks is a Medical Toxicologist and risk assessment expert with more than 30 years of experience in academia, industry and the health service. He is Adjunct Professor of Toxicology at the University of Basel. From 2009 to 2023 he has been the Director fo the Swiss Centre for Applied Human Toxicolgoy (SCAHT) and from 2012 to 2023 Adjunct Professor at the University of Geneva. He is a EUROTOX Registered Toxicologist, a Fellow of the Royal College of Physicians of Edinburgh, Secretary-General of EUROTOX and President-elect of the International Union of Toxicology (IUTOX).
morelessParticipation Fee: € 995.00 plus VAT.
The registration fee includes the following benefits:
Representatives of an authority or a public university are therefore eligible for a reduced fee of € 595.00 plus VAT per person (please provide evidence). The reduced fee cannot be combined with other rebates.
Group Reductions
For joint bookings received from one company we grant a 15% discount from the third participant onwards.
Terms of Cancellation / Book without Risk
You can cancel your participation in our online events free of charge and without giving reasons in writing up to 1 week before the start of the event. In the case of later cancellations and non-login to the online event, no participation fees can be refunded.
In this case, however, you will receive access to the documentation after the event.
You can name a substitute participant free of charge at any time.
Would you have liked to attend this event, but cannot spare the time?
For the price of 295,00 € plus VAT you can order a complete set of event documentation. A few days after the event you will receive the access data for the restricted download section of our Website. There you will find all presentations (subject to the approval of our speakers) as pdf-files.
Sabine Mummenbrauer
Programme and conceptual design
+49 231 75896-82
smummenbrauer@akademie-fresenius.de
Sabine Mummenbrauer
Programme and conceptual design
+49 231 75896-82
smummenbrauer@akademie-fresenius.de
Sabine Mummenbrauer
Programme and conceptual design
+49 231 75896-82
smummenbrauer@akademie-fresenius.de
Alexandra Schardt
Organisation and participant management
+49 231 75896-74
aschardt@akademie-fresenius.de
Alexandra Schardt
Organisation and participant management
+49 231 75896-74
aschardt@akademie-fresenius.de
Present your Company at the Event.
You can personally present your products and services directly to your specified target group. We are happy to provide you with further information on our range of available options – from displaying company information at the reception counter to presenting your company with an exhibition stand.
We would be pleased to assist you personally:
Monika Stratmann
Phone: +49 231 75896-48
info@akademie-fresenius.de
We offer journalists and editors a platform where they can get in touch with the experts.
If you are the editor of a specialist publication and interested in a press pass or media partnership, please contact us well in advance. We are happy to advise you.
Please contact us:
Katharina Geraridis
Phone: +49 231 75896-67
presse@akademie-fresenius.de
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