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
ECHA has launched a consultation on the proposed REACH restriction of Octocrylene in cosmetics. Learn what the proposal means for manufacturers, formulators and regulatory teams.
Recevez une fois par mois les dernières actus réglementaires et conseils d’experts.
A study on a pizza box reveals toxic substances in food packaging. The lack of knowledge on these substances poses a challenge for regulators and industries. Will there be an increase in controls on materials in contact with food products?
The Candidate List has been updated with 10 new substances, bringing the total to 191. Substances like D4, D5, and lead have been added due to their harmful effects on health and the environment. Learn more about the Candidate List and its purpose.
Learn about the "same" biocidal product Marketing Authorisation (MA) process, from wider to narrower authorisations or markets. Find out how to submit a dossier, the evaluation process, supporting documents, and linked fees. Explore more on biocidal products' regulation in Europe.
The simplified authorisation procedure promotes the use of environmentally friendly biocidal products by ensuring they meet specific criteria, such as containing no substances of concern or nanomaterials. Once authorised, these products can be marketed across Member States with minimal fees.
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.
