Day 1
The presentations given during the first day can also be watched on our YouTube channel.
13:00 | 15 min | Introductory presentation: How to address systemic health effects with non-animal methods? - Gaps, overlaps and research needs | Elisabet Berggren (EU Commission, JRC) |
13:15 | 10 min | A national risk assessor's perspective to move towards the assessment of systemic health effects using non-animal methods | Christophe Rousselle (ANSES, France) |
13:25 | 10 min
| How are human health systemic effects covered when animal testing is not allowed? | Qasim Chaudhry (SCCS) (online) |
13:35 | 10 min | What does it take to start reducing systemic animal testing now, and to phase it out soon? | Heli Hollnagel (CEFIC LRI) |
13:45 | 10 min
| Paving the way towards a One-Health approach to chemical risk assessment | Julia Baines (PETA) |
13:55 | 10 min | An initiative towards a future solution: the EPAA Designathon | Carl Westmoreland (EPAA) |
14:05 | 55 min | Panel discussion | Moderator: Elisabet Berggren Panellists:
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15:20 | 15 min | Introductory presentation: Long-term aquatic toxicity as area of concern – current regulatory status - differences between legislative areas | Georg Streck (EU Commission, DG GROW)
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15:35 | 15 min | How to address fish aquatic toxicity with alternative approaches? – Possibilities, gaps and challenges to be addressed | Adam Lillicrap (Norwegian Institute for Water Research) (online) |
15:50 | 15 min | NGRA for the aquatic environment | Stephanie Bopp (EU Commission, JRC) (online) |
16:05 | 15 min | Presentation by a MS authority on their view how to replace fish long-term toxicity testing | Gerd Maack (Environment Agency, UBA) |
16:20 | 15 min | Feedback from the EPAA Partner Forum: Possibilities to address the area of long-term aquatic toxicity | José Vicente Tarazona Lafarga (Instituto de Salud Carlos III) |
16:35 | 55 min | Panel discussion
| Moderator: Marco Fabbri Panellists:
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Day 2
You can also watch the presentations and discussions during the second day on our YouTube channel.
Part 1 Setting the scene | |||
12 December, 9:00 | 10 min | Introductory presentation on | Katrin Schutte (EU Commission, DG ENV) |
9:10 | 15 min | Different needs of legislative areas
| Katrin Schutte (EU Commission, DG ENV) |
Part 2 Validation – how can it evolve | |||
9:25 | 10 min | Joao Barroso (EU Commission, JRC) (online) | |
9:35 | 10 min | OECD stakeholders’ survey and workshop on operational and financial aspects of validation | Anne Gourmelon (OECD) |
Part 3 Acceptance for regulatory use | |||
9:45
| 15 min | PARC NGRAroute – a roadmap for making EU chemicals legislation NGRA-ready | Matthias Herzler (German Federal Institute for Risk Assessment, BfR) |
10:20 | 10 min | Pathways to regulatory acceptance - Looking beyond validation | Andrew Worth (EU Commission, JRC) (online) |
10:30 | 10 min | Experiences from the US-Roadmap to regulatory acceptance of non-animal methods | Nicole Kleinstreuer (NICEATM/ICCVAM) (online) |
10:40 | 55 min | Panel discussion | Moderator: Miriam Jacobs (UK Health Security Agency) Panellists:
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11:35 | 50 min | Panel discussion:
| Moderator: Gavin Maxwell (EPAA) Panellists:
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12:25 | 5 min | Wrapping up/next steps | Georg Streck (EU Commission, DG GROW) |
12:30 | 5 min | Closing remarks | Cristina de Avila (EU Commission, DG ENV) |
12 December, 12:35 |
| End of the first part of the workshop |
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