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 reporting requirements for poison centres under Annex VIII of the CLP Regulation. Find out who is affected, the UFI code, notification deadlines, and how to comply with the new obligations. Stay informed and prepare now for upcoming deadlines.
A study by ECHA reveals that most European companies are substituting harmful substances, driven by regulatory measures like REACH restrictions and authorisations. Consumer demand, corporate image, and sustainability policies also significantly influence this shift towards greener alternatives.
The new Medical Devices Regulation (EU Regulation 2017/745) has been postponed to May 2021 due to Covid-19. Changes in classification rules and broader scope will impact businesses. Borderline products require vigilance, and all medical devices must be re-certified by 2024.
Learn about the new Cosmetics Supervision and Administration Regulation (CSAR) in China. Changes include new cosmetic definitions, simplified ingredient registration, and classification updates. Stay informed and register for an upcoming webinar on the topic.
ECHA plans to screen all REACH registration dossiers by 2027 to prioritize chemical risk management, assess low-priority substances, and identify those needing more data. Compliance checks will cover 30% of substances, emphasizing the importance of keeping dossiers updated.
Learn about the 22 new substances added to the PIC Regulation in July 2020, requiring export notification. Find out more about this regulation and its impact on European companies exporting hazardous chemicals.
