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
Many CEPA compliance risks arise from overlooked operational obligations. Learn which reporting, recordkeeping, and notification duties companies often underestimate.
Recevez une fois par mois les dernières actus réglementaires et conseils d’experts.
Home fragrances (candles, incense, diffusers, room sprays) are increasingly scrutinized for VOC emissions and potential impacts on indoor air quality. This article clarifies why “natural vs synthetic” is a misleading safety proxy: what matters is the risk of the finished product—hazard combined with real-world exposure under foreseeable use. It highlights why emissions vary widely across product types, formulations, and usage conditions (combustion, ventilation, duration), and connects the risk assessment approach to EU Regulation 2023/988 on general product safety.
An overview of CEPA requirements for organizations operating in Canada. Learn key obligations, compliance responsibilities, and best practices across all sectors.
Managing cosmetic compliance across multiple markets quickly becomes complex when relying on spreadsheets. This article examines the limits of manual data management and when a more structured approach becomes necessary.
Managing cosmetic regulatory data across the U.S., Canada, and Europe is no longer just a compliance issue. It is a data management challenge that directly impacts consistency, risk, and scalability for cosmetic brands.
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.
At the end of 2025, the Biocidal Products Committee failed to reach a consensus on the approval of ethanol as a biocidal active substance, pushing its opinion back to May 2026. This delay effectively extends the transitional period but leaves manufacturers and importers facing ongoing uncertainty when planning their product portfolios and authorisation strategies.
