Safety, Health & Environment (SHE)

The Fecc SHE Committee is the leading expertise hub for Safety, Health, and Environmental excellence within the European chemical distribution sector. We drive industry standards by proactively navigating the complex EU regulatory landscape, ensuring that chemical storage, workplace safety, and environmental protection remain at the forefront of every member’s operations. By bridging the gap between high-level legislation and day-to-day operational reality, we empower our members to achieve the highest standards of safety and corporate responsibility.

The Fecc SHE Committee functions as an expert-led forum that monitors, evaluates, and influences the European legislative landscape. We work in direct partnership with the European Chemicals Agency (ECHA) and the European Commission to ensure that safety and health regulations are practical, science-based, and effective for the distribution sector. Our primary focus remains the ongoing optimization of REACH and CLP frameworks, alongside emerging sustainability mandates. By leveraging the collective knowledge of our member experts, we provide the essential foresight needed to protect human health and the environment while fostering a resilient, competitive chemical supply chain.

The Fecc SHE Committee provides expert monitoring and technical guidance on the most critical EU legislative developments. Our current priority is assisting members with the 2026 implementation of the REACH microplastics reporting obligations and the transition to new CLP hazard classes (including Endocrine Disruptors and PMT/vPvM substances). We facilitate the exchange of best practices regarding the Seveso III Directive for chemical storage and the shift toward the Industrial Emissions Directive (IED 2.0). By aligning our work with the EU Zero Pollution Action Plan and the “One Substance, One Assessment” (OSOA) framework, we ensure that distributors stay ahead of the curve in hazard control, workplace safety, and environmental stewardship.

PFAS & “Essential Use” Strategy

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The universal restriction proposal for per- and polyfluoroalkyl substances (PFAS) represents a transformative challenge for chemical distributors, who sit at the heart of the European supply chain. As the EU moves toward a broad ban under the “essential use” principle, distributors must move beyond simple logistics to become strategic advisors for their customers. This involves conducting exhaustive portfolio audits to identify PFAS-containing products—from high-performance lubricants to specialized surfactants—and managing the risk of sudden supply chain disruptions as manufacturers begin to phase out these substances.

The committee’s primary focus is to help distributors navigate this transition by providing clarity on complex derogation timelines and the availability of sustainable alternatives. We empower our members to proactively communicate with both upstream suppliers and downstream users, ensuring that the shift away from “forever chemicals” is handled with technical precision and does not compromise the operational stability of the industries they serve.

ECHA – PFAS Restriction Proposal

Watch here the webinar “PFAS restriction: ECHA Committees’ opinions and next steps” on 07/05/2026 | 11:00 – 12:40.

Following the publication of the final opinion of the Committee for Risk Assessment (RAC) and the draft opinion of the Committee for Socio-Economic Analysis (SEAC) on the per- and polyfluoroalkyl substances (PFAS) restriction proposal on 26 March, we will host a webinar presenting the key elements of both opinions.

The webinar will explain the conclusions reached so far by the two committees, on the hazards, emissions and risks of PFAS, the risk reduction potential of the proposed restriction and the socio-economic impacts, including the availability of alternatives and possible derogations. It will also outline the next steps in the REACH restriction process.

 

 

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New CLP Hazard Classes

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The update to the CLP Regulation introduces new hazard classes—including endocrine disruptors (ED) and persistent, mobile, and toxic substances (PBT, vPvB, PMT, and vPvM)—that directly impact the daily operations of chemical distribution. For a distributor, these new criteria mean more than just updated labels; they trigger a ripple effect across inventory management, warehouse safety protocols, and the legal accuracy of Safety Data Sheets (SDS) for imported or relabeled products.

Our key objective is to provide distributors with the tools to manage this massive reclassification process across diverse product ranges. We focus on clarifying the specific legal deadlines for mixtures and substances, helping members understand how these new classifications may lead to broader restrictions or changes in transport requirements. By simplifying these regulatory complexities, we ensure that distributors remain compliant while continuing to provide the high level of safety information and reliability that their customers depend on.

New hazard classes 2023 – ECHA

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Watch here the webinar “Introduction to ECHA’s guidance on new CLP hazard classes”.

Are you impacted by the classification of substances under the CLP Regulation? This webinar gives an overview of the new ECHA guidance on the recently introduced hazard classes under the Classification, Labelling and Packaging (CLP) Regulation.

The updated guidance has been developed by experts from ECHA, EU Member States, EU level non-governmental organisations and associations as well as other nominated experts. The guidance outlines the new hazard classes for endocrine disruptors, Persistent, Bioaccumulative and Toxic or Very Persistent, Very Bioaccumulative (PBT/vPvB), and Persistent, Mobile, and Toxic or Very Persistent, Very Mobile (PMT/vPvM) properties. These additions aim to better protect human health and the environment by addressing emerging concerns in chemical safety.

During the webinar, we will discuss the protection goals and the classification criteria for the new hazard classes, as well as the development of the associated CLP guidance. You will also learn about the regulatory timelines and how ECHA manages the related administrative process once proposals for harmonised classification and labelling are submitted.

 

 

 

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