NIA's Director of Regulatory Affairs sat in on the inaugural meeting of ECHA's Collaborative Platform of Alternatives to Animal Testing (CP-AAT), a new group backing the European Commission's push to phase out animal testing in chemical safety assessments. The platform draws in EU Member States, the Commission, EU agencies, industry, academia and public-private partnerships, all working to speed up regulatory acceptance of non-animal methods. Members used the first session to map existing European work in this space and settle on four priorities for the coming two years, and the group will meet twice yearly going forward to keep initiatives coordinated and avoid duplicated effort. NIA members can request more detail on the projects under discussion.
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NIA Regulatory Committee in 2026
The NIA Regulatory Committee has already outlined several priority topics for this year’s discussions. These include: Reviewing developments under REACH once the new proposals are announced. Exploring how nanomaterials fit within the One Substance, One Assessment framework. Examining the role of nanomaterials in UK REACH. Following updates to the Safe and Sustainable by Design (SSbD) framework. If Members have additional topics they would like the Regulatory Committee to address, please contact…
Read MoreNIA Brings Industry Perspective to SSbD25 Discussions in Zurich
NIA’s Director of Regulatory Affairs, Blanca Suárez-Meriño, took part in the final panel discussion at the SSbD25 Conference in Zurich, sharing the industry’s perspective on Safe and Sustainable by Design (SSbD). The panel also featured representatives from the European Commission, Cefic, EMERGE, and IVL. Discussions focused on how SSbD principles can be integrated into early-stage innovation — marking a shift in mindset from add-on practices to embedded approaches — and on the importance of…
Read MoreNIA Contributes to Key Discussions at Nanomaterials Expert Group 20
On the 8th of November NIA Director of Regulatory Affairs, Dr Blanca Suarez Merino, attended the 20th meeting of the Nanomaterials Expert Group (NMEG) remotely, where technical issues relating to the implementation of REACH, CLP, and the Biocidal Products Regulation (BPR) for nanomaterials are discussed. As a permanent stakeholder representative, NIA took the opportunity to raise questions and issues brought forward by its members. Further information on the event is available to members…
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