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
Active substance renewal under the GB Biocidal Products Regulation (GB BPR) is a critical regulatory challenge for companies placing biocidal products on the Great Britain market. With strict 550-day submission deadlines and major expiries in 2026 and 2027, early planning is essential to avoid market disruption and loss of product authorisations.
Recevez une fois par mois les dernières actus réglementaires et conseils d’experts.
Learn about the requirements for labeling products as Cruelty-Free in Europe, the evolution of animal testing laws, and the importance of compliance for imported cosmetics. Stay informed to avoid false claims and ensure your products meet regulations.
Learn about the process of obtaining marketing authorisation for biocidal products at national and European levels. Discover the different types of authorisations, including Union, National, and Simplified, and understand the requirements and timelines involved in each.
Learn about the post-registration processes for REACH compliance. Understand the criteria for dossier completeness, compliance checks, substance evaluation, and more. Stay updated, communicate with your supply chain, and ensure compliance to avoid extra costs.
EcoMundo presents you with 4 key points for successfully conducting your Alternatives Analysis, a crucial step in the creation of the Authorization dossier.
Learn how to navigate REACH regulations if you haven't registered your substances yet. Discover loopholes, tonnage band calculations, and what to do if you create a new substance post-May 2018 deadline. Plus, find out about exemptions and recommendations for compliance.
Learn about the 4 exceptional cases identified by ECHA where registrants may struggle to submit a complete registration dossier on time. Find out how to inform ECHA of your situation and what evidence to provide by the deadline.
