Modular Solution for Cosmetics Compliance
Check the Conformity of your Formulas
Secure your regulatory documents for each zone
Optimize on-site risk management
Manage your Safety Data Sheets efficiently
Automate your regulatory monitoring
Ensure the traceability of your substances
Maintain good HSE risk management
After more than twenty-five years of negotiations, the European Union and the Mercosur countries — Brazil, Argentina, Uruguay and Paraguay — finalized their trade agreement. Provisionally applied since 1 May 2026, the agreement marks a major step in economic relations between Europe and South America. For European companies in cosmetics, fragrance and home fragrance, the issue is twofold: benefiting from progressively improved commercial access to high-potential markets, while continuing to comply with regulatory requirements that remain largely national. Although the EU–Mercosur agreement creates new opportunities, it does not remove product registration obligations, labelling requirements or the need for a local responsible party in the countries concerned. For European brands, success will depend not only on commercial strategy, but also on early regulatory planning.
Recevez une fois par mois les dernières actus réglementaires et conseils d’experts.
SCCS issues final opinion on homosalate as a UV filter in sunscreen products, recommending a maximum concentration of 0.5%. The SCCS also addresses endocrine disrupting properties of homosalate. Learn more about SCCS evaluations and stay compliant with cosmetic regulations.
The European Commission has updated the REACH regulation, setting specific deadlines for registration dossier updates. ECHA's compliance checks target Annex XIV substances lacking authorization dossiers. New rules clarify information requirements, enhancing transparency and predictability.
The European Commission has proposed 5 new substances for inclusion in Annex XIV of the REACH Regulation, subject to authorization. Companies using these substances must find alternatives or submit an authorization dossier.
ECHA added 8 new substances to the Candidate List for authorisation, bringing the total to 219. Learn about the new entries and the obligations that arise when substances are classified as SVHCs.
Learn about your obligations under SCIP if you are a European supplier of articles containing SVHC substances. Find out when to update your SCIP notification and what information to provide. SCIP aims to make information on hazardous substances available to waste managers and consumers for safer product disposal.
Understanding the compliance of medical devices with new regulations can be complex and costly. Companies need to invest time and resources in various aspects such as training, market surveillance, and continuous data collection. Working with a specialist consultant can help navigate these challenges and ensure product compliance. Learn more about the impact of Regulation 2017/745 and the importance of post-marketing surveillance in this blog.
