EcoMundo's Blog

British companies with EU REACH Authorisations must obtain UK REACH Authorisations post-Brexit. They need to inform the HSE within 60 days and provide technical information. Downstream users must also notify HSE.

ECHA extends Brexit window until 12th April, giving companies more time to appoint an Only Representative in the EU-27. Transfer your REACH responsibilities now to avoid losing registrations and authorizations post-Brexit. Prepare for Brexit now to avoid last-minute rush.

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.