REACH Revision Roundtable

REACH Revision Roundtable

This roundtable will explore the recent REACH Revision proposal and its impact on industry, with expert insights from toxicology, legal, and economic perspectives. Participants will gain a clearer understanding of the revision’s im­plications and have the opportunity to engage directly with the panel through live Q&A.

Informace

  • Date: 21st May 2025
  • Time: 10:00 AM CEST
  • Location: ZOOM platform

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The European Commission's newly proposed REACH Revision has stirred significant discussion across the chemicals industry. Introduced during CARACAL-54, the proposal seeks to strengthen safety measures, increase transparency, and modernize how chemical data is shared across the supply chain. However, with changes such as proposed time-limited registrations, stricter update obligations, and alignment with updated hazard classes and classification obligations under CLP, many in the industry are raising concerns about feasibility, proportionality, and overall burden.

To address these questions, we are convening a virtual roundtable featuring diverse expert voices – from toxicology, legal policy, and industry representation. The session is designed to unpack what the REACH Revision really means for companies operating under EU chemical legislation.

Whether you're part of a regulatory affairs team, a compliance officer, or a business decision-maker navigating EU chemicals policy, this discussion will provide context, critical perspectives, and space for interactive Q&A with experts.

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Moderator: Tomas Novotny

REGARTIS

Tomas graduated from Applied informatics in Chemistry at the University of Chemistry and Technology in Prague. He is the owner and a Customer happiness manager in REGARTIS. Tomas is a senior expert in the field of EU chemicals legislation (REACH, CLP), business strategy expert, and communication wizard enabling the most effective cooperation between our technical experts and customers. Tomas is also often leading scientific projects for ECHA, EFSA, and JRC.

Panelists:

Marko Susnik

Austrian Economic Chamber (WKÖ) & SMEunited

Marko Sušnik is an advisor for chemical law and chemical policies within the Austrian Federal Economic Chamber (WKÖ – Wirtschaftskammer Österreich). He is involved with REACH, CLP, national chemical law, nanotechnologies, biocides, pesticides and fertilizers. On the European level he works in numerous expert groups related to chemicals. His work is very much focused on the impact of European legislation on SME. In that context he is also advising the European social partner SMEunited, the European Association of Craft, Small and Medium-Sized Enterprises, on aspects related to chemical legislation and policy. From his professional training he is a chemist, specialized on organic chemistry and organic technologies. He finished his chemical education with a PhD in chemical engineering.

Ales Bartl

Keller and Heckmann LLP

Ales Bartl has a broad experience in EU product regulatory law, including REACH, Classification, Labelling, and Packaging (CLP) regulation, Biocidal Products Regulation (BPR), medical devices, electronic products, and general product compliance and product safety. He advises on regulatory compliance of a broad range of products marketed in the EU and represents clients before EU and national competent authorities on compliance and enforcement issues, including product withdrawals and recalls. Ales also represents clients before the Court of Justice of the European Union and the Board of Appeal of European Chemicals Agency.

Adam Jonas

REGARTIS

Adam is our toxicology and ecotoxicology expert. He is involved in this field since 2007. He started in academia performing experimental work to investigate the endocrine activity, acute toxicity, and neurotoxicity of various substances, mixtures, or environmental samples. He published several articles in leading toxicology and ecotoxicology journals. Later he had several regulatory roles in industry focused on biocides, plant protection, REACH, and CLP in the EU and other regions with proven track of successful registrations. He has experience with the endocrine disruptors assessment of plant protection and biocidal active substances under the current EFSA and ECHA guidance. He also helped to designed and study monitored numerous toxicological and ecotoxicological studies very often with very specific and difficult to be tested substances.