Modular Solution for Cosmetics Compliance
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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.
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.
In order to ensure that businesses in the United Kingdom remain in compliance with the REACH regulation, the competent British authorities have put in place various approaches to analyze the substances and sectors where the most likely risks would be likely to occur. Their aim is to ensure that all companies that have pre-registered with ECHA finalize their procedure before the REACH 2018 deadline.