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 3 registration deadlines set by REACH for chemical substances, the changes it brought to industrial practices, and what to expect next in terms of chemical safety regulations in the EU. Stay compliant and keep up with evolving requirements.
Learn about the national marketing authorisation process for products in a single state, including mutual recognition procedures, dossier submission, evaluation, and supporting documents. Understand the role of competent authorities and the potential fees involved.
EcoMundo excels in assisting companies with REACH Authorisation requests, with a 100% success rate since 2015. Their team offers expert guidance, adaptability, unique methodology, and ongoing support for a successful outcome.
Union authorisation allows companies to market biocidal products across the EU with a single approval, bypassing national authorisations. The process involves dossier submission, evaluation by competent authorities, and a final decision by the European Commission.
Learn about the requirements for labeling products as Cruelty-Free in Europe, the evolution of animal testing laws, and the importance of compliance for imported cosmetics. Stay informed to avoid false claims and ensure your products meet regulations.
Learn about the process of obtaining marketing authorisation for biocidal products at national and European levels. Discover the different types of authorisations, including Union, National, and Simplified, and understand the requirements and timelines involved in each.
