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
In 2025, cosmetic, fragrance and home fragrance compliance has shifted to true global-by-design: brands must build products to meet EU, US, Canadian and emerging market (Taiwan, ASEAN, GCC) requirements from day one. EcoMundo’s blog explains this growing regulatory complexity—dermocosmetics, hair “skinification”, perfumes, digital tools & PLM—and shows how to secure ingredients, structure product files (PIF, DIP) and industrialize global compliance to stay competitive into 2026.
Recevez une fois par mois les dernières actus réglementaires et conseils d’experts.
The OECD has established guidelines for chemical testing to ensure safety. PEPPER, a program under SNPE, aims to fill gaps in endocrine disruptor qualification and regulation. Learn more about these initiatives and their importance in ensuring chemical safety.
The European Commission proposes restricting D4, D5, and D6 in cosmetics to protect the environment from their harmful, bioaccumulative effects. The regulation, set for adoption by the end of 2023, aims to reduce emissions and promote sustainable practices in the cosmetics industry.
Learn about the latest IFRA standards impacting cosmetic and homecare products. Discover new restrictions and additions to perfume ingredients. Find out about the transition period and how to stay compliant with the updated standards.
Learn the difference between dietary supplements and medications, and the risks associated with using medicinal plants in supplements. ANSES has developed a tool to help healthcare professionals inform consumers. Visit their website for more information.
The European Commission has authorized specific uses of 4-tert-OPnEO and 4-NPnEO, substances of very high concern, for in vitro diagnostic and life science kits until 2031. These substances, used in various industrial and medical applications, are listed due to their environmental risks.
New information requirements for REACH registration dossiers have been implemented by ECHA. Changes include substance identity and standard information requirements. ECHA aims to control substances registered above 1t/year by 2027. Additionally, ECHA has added 2 new substances to the SVHC candidate list.
