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
Learn the key differences between US and EU cosmetic regulations and how to export your products from the USA to Europe in full compliance.
Recevez une fois par mois les dernières actus réglementaires et conseils d’experts.
A draft regulation proposes adding 12 new substances to the REACH Annex XIV Authorisation List, pending approval by the European Parliament and Council. This list restricts the use and marketing of certain substances in the EU unless authorised.
Companies selling substances in the UK must register under UK REACH, similar to EU REACH. UK-based holders of EU registrations need to validate them post-Brexit. Different roles, such as EU manufacturers and UK importers, have specific requirements to ensure compliance.
Learn about cGMP regulations for drug products, including FDA compliance and consequences of non-compliance. Understand 21 CFR Part 210 and 211, and how to ensure cosmetic compliance in the US. Contact our experts for more information.
Post-Brexit, UK companies must transfer biocidal product authorizations to an EU-27 country to remain valid. UK suppliers need EU-based representatives, and ongoing evaluations must be transferred. Simplified authorizations will require new applications.
Learn about the pre-registration process for existing substances in South Korea under K-REACH. Find out why pre-registering is important, who is affected, and how to prepare for the June 30th deadline.
Stay compliant with EU-27 regulations post-Brexit by designating a Responsible Person within the EU for UK-based cosmetic companies. Ensure proper CPNP notifications, maintain updated PIFs, and adapt product labeling to meet both EU and UK standards, especially in Northern Ireland.
