EU-ToxRisk Virtual Open Symposium
23-24 February 2021
OBJECTIVES OF THE MEETING
PROGRAMME
The programme of the Open Symposium is divided into a total of 5 public sessions, followed by 1 closed session, which is restricted to EU-ToxRisk members, RAB, SAB. The sessions will cover two afternoons:
DAY-1, Tue 23 Feb 2021 (13:00 - 17:30pm CET)
DAY-2, Wed 24 Feb 2021 (13:00 - 17:30pm CET)
Documents supporting the event programme (available for download in the "FILES" section further down):
For more information on the EU-ToxRisk project Case Studies, please visit the Case Study section on our public project website, here.
VIRTUAL MEETING ROOM
The Open Symposium is organised as an online event:
REGISTRATION
QUESTIONS
If you have any questions regarding this event, or issues with registration, please contact the Project Office.
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This project has received funding from the European Union’s Horizon 2020 Research and Innovation Programme under Grant Agreement N° 681002.
13:00 - 14:20 | Session 1: Release of the EU-ToxRisk Advisory Document on NAM-enhanced read-across | |
Key features of the Advisory Document on how to effectively apply NAM-enhanced read-across for risk assessment, as developed by the consortium and its stakeholders. - Chair: Sylvia Escher (ITEM) |
14:40 - 17:30 | Session 2: Round-2 case studies – new challenges for NAM-based risk assessment | |
Presentation of the results from a new set of EU-ToxRisk case studies. These new studies address relevant regulatory and scientific questions of broad impact, including: testing of chemicals with little or no observed adverse effects; testing of chemicals inducing multi-target organ toxicity; testing of metabolism-activated toxicants; exploring ab initio testing strategies. - Chair: Bob van de Water (UL) |
13:00 - 14:40 | Session 3: Next-generation risk assessment by new-generation scientists | |
Speed presentations of the latest science carried out in the project, with a focus on High-throughput transcriptomics-based testing methods (HTTr) and functional genomics to uncover mode-of-action & Innovative in silico and in vitro NAMs for Next Generation Risk Assessment. - Chair: Paul Jennings (VU) |
15:00 - 16:15 | Session 4: Validation strategies for NAMs | |
Podium discussion with stakeholders on suitable validation strategies for NAMs to support regulatory acceptance and uptake. - Chair: Ian Cotgreave (RISE) |
16:30 - 17:30 | Session 5: EU-ToxRisk sustainability | |
EU-ToxRisk commercialization platform for integrated testing; follow-up projects RISKHUNT3R and the European Partnership for Chemical Risk Assessment (PARC). - Chair: Marcel Leist (UKN) |
17:30 - 18:30 | Closed session: Feedback from the EU-ToxRisk SAB/RAB to the project consortium | |
<< EU-ToxRisk partners, SAB, RAB only >>
Feedback from the SAB and RAB and conclusive remarks. - Chair: Bob van de Water (UL) |
EU-ToxRisk Project Office
EU-ToxRisk Project Office: eu-toxrisk-arttic@eurtd.com