Cosmetic, Biocide or a Medicinal Product? An EU and US comparison
Deciding whether a product is classed as a cosmetic, biocide or medicinal product can be a complex task. Many products have dual purposes such as antibacterial hand washes and as such can fall under different regulations.
Our new whitepaper by Dr Stacey Webster aims to provide guidance on borderline products within Europe and provide a comparison to the United States with an emphasis on soaps, hand washes, cleansers and wipes.
Download the “Cosmetic, Biocide or a Medicinal Product? An EU and US Comparison” Whitepaper and other great resources here.
Explore the key facts about Dechlorane Plus in this concise Q&A. From its uses and environmental impact to regulatory concerns, we answer the most pressing questions to help you stay informed.
The Corporate Sustainability Reporting Directive (CSRD) will introduce significant changes starting in January 2025, greatly expanding its scope. Companies need to act promptly to ensure compliance, avoid potential penalties, and position themselves as leaders in sustainable business practices. Learn how Yordas Group can help support your journey to compliance.
Despite the rigorous framework, non-compliance in SDS remains a prevalent issue. This often falls into four categories: Incomplete, Incorrect, Inappropriate, or Inconsistent information. Learn more here.
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.