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 new EU regulation mandates that all CE-marked products sold in Europe must have an authorised representative based in the EU from 16th July 2021. This affects companies selling products manufactured outside the EU, including the UK, and requires compliance with safety standards.
From 1st January 2021, companies must notify hazardous mixtures in a new harmonised format. This blog explains the requirements and deadlines for compliance with the CLP Regulation. Learn about generating UFIs and why harmonisation is important for poison control centres.
The AGEC law, effective in France since 2021, aims to reduce waste and improve consumer information, impacting industries like cosmetics. Key measures include phasing out single-use plastics by 2040 and requiring detailed packaging labels, sparking manufacturer concerns.
Color additives are the only cosmetic ingredients in the United States that require pre-market FDA approval. This article shows you the main points to consider when launching a cosmetic product that contains color additives.
Despite significant costs to businesses, REACH authorisation offers substantial benefits, including improved health and environmental protection, reduced use of hazardous substances, and promotion of innovation. The societal benefits far outweigh the health risks.
Disinfectants can be classified as either medical devices or biocides based on their use. Medical device disinfectants are used for non-sterilizable reusable devices and must comply with EU Regulation 2017/745, while biocides follow EU Regulation 528/2012. Understanding the correct classification is crucial for compliance.
