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.
Learn about the deadlines for registering pre-registered substances under K-REACH in South Korea. Find out the grace periods and requirements for new substances. Discover how the registration process works.
Navigating the complex process of marketing biocidal products in the EU requires submitting a Biocidal Product Marketing Authorization dossier. Companies can reduce costs by joining consortia to share resources and expertise, ensuring compliance with the Biocidal Products Regulation.
Discover key insights from the Biocides Congress, including updates on the French PNSE4, DGCCRF findings, and Afise's Chemical Strategy for Sustainability.
Amazon now requires sellers to provide a certificate of compliance for food supplements in the EU. Learn about regulations, labelling, and variations between Member States.
Explore the expanded scope of the new Medical Device Regulation (MDR), which now includes non-medical devices, and understand the importance of determining your device's risk class. Learn about compiling technical documentation, choosing a notified body, and implementing post-marketing follow-up.
Learn about the key obligations for marketing toys in the EU, including compliance with Directive 2009/48/EC, safety assessments, labeling requirements, and CE marking. Understand the importance of technical documentation and adherence to testing standards for toy safety.
