Assurez la conformité réglementaire de vos produits
Vérifiez la conformité de vos formules
Vérifiez et sécurisez vos documents réglementaires pour chaque zone.
Optimisez la gestion des risques sur site
Gérez efficacement vos Fiches de Données de Sécurité
Automatisez votre veille réglementaire
Assurez la traçabilité de vos substances
Pérennisez la bonne gestion des risques HSE
Join us for a comprehensive webinar dedicated to exploring the key aspects of the REACH regulation.
Recevez une fois par mois les dernières actus réglementaires et conseils d’experts.
Explore the innovations shaping the future of detergents.Decode regulatory implications to ensure compliance (with both current and revised regulations). And Identify effective strategies to turn these developments into competitive advantages.
This webinar is dedicated to food supplement claims and their variety (nutritional, beauty, health...) and aims to provide the essential keys for classifying each type of claim to properly define what is legally permitted.
Our experts explain the key points of an SDS to be diffused in the European Union, as well as the new requirements for the year 2023, in order to avoid pitfalls when creating your document.
In this webinar, we will discuss the obligations according to the different roles in the supply chain, we will also guide you through the different steps in order to perform the SCIP notification.
Biocidal active substances are called in situ generated active substances if they are generated from one or more precursors at the place of use. The approval of these substances requires evaluation of the generated active substance and of the precursor(s) it is generated from, in the context of each product type (PT).
All biocidal products must comply with certain regulatory provisions before being placed on the European market (Biocidal Products Regulation 528/2012). They depend on the status of the active substance, the product type (PT) and the Member State(s) in which the biocidal product will be made available.
After Brexit on 31 January 2020, the UK entered a time limited transition period until 31st of December 2020. As the transition period has ended, regulation is an autonomous matter for both the UK and the EU as 2 separate legal and regulatory systems.
Companies must register substances and, in order to do so, collaborate with other companies that register the same substances. In this webinar, we will review the principles of REACH registration, explaining the scope, progress and obligations in the supply chain.
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