The European Council has officially adopted long-awaited updates to the CLP Regulation, a critical component of the EU’s Chemicals Strategy for Sustainability. This development represents a major step forward in enhancing consumer safety. Learn more here.

 Suppose your company is placing hazardous mixtures on the EU market. In that case, ensuring your PCN submissions are fully compliant is crucial—especially as enforcement authorities ramp up efforts to audit notifications and ensure adherence to regulations. Is your business ready? Find out here.

As companies outside the EU navigate the landscape of Poison Centre Notifications (PCN), understanding submission requirements is essential for compliance and market access. This article addresses frequently asked questions regarding the submission obligations for non-EU legal entities.

With the approach of the January 1, 2025, deadline for Poison Centre Notifications (PCN), businesses must understand the distinct submission requirements across the EU, Great Britain (GB), and Northern Ireland (NI). This article addresses frequently asked questions regarding the differences in these requirements.

Whether you are submitting for the first time or managing existing dossiers, understanding when and how to update a PCN submission is essential for continuous compliance. Our team answers some frequently asked questions to help you navigate the PCN submission process.

On 23 July 2024, the Ukrainian Government published a Resolution on the approval of Technical Regulation (commonly known as “Ukraine REACH”). Here's everything you need to know about what to expect.

With the EU Poison Centre Notification (PCN) deadline for industrial mixtures approaching rapidly, many businesses are struggling with regulatory requirements and processes. Our team answers some frequently asked questions to help you navigate these complex requirements.

Environmental or ‘green’ claims are statements made by companies about the environmental benefits or attributes of their products (goods and services). Learn more about them in our Q&A.

Enjoy reading our interview with Yordas auditors about their team and the services they provide to our clients.

With the rapidly changing nature of the PFAS regulatory landscape, it’s important to stay on top of changes and updates. Following our last Q+A, here are more key PFAS questions that our experts have answered.

Navigate the complex landscape of chemical regulation in South Korea and learn how your business can stay ahead of upcoming changes and deadlines.

A “same biocidal product” is a regulatory concept introduced under EU BPR through an amendment regulation (Commission Implementing Regulation (EU) 2016/1802). Under this process, an applicant may submit their own biocidal product authorisation application for a product which is authorised or under evaluation for authorisation. Learn more here.