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
In this webinar, we will guide you through the key steps to successfully submit a Biocide Authorisation dossier in Europe.
Recevez une fois par mois les dernières actus réglementaires et conseils d’experts.
Discover the essentials of an SDS to communicate clearly with your customers and evaluate the quality of those provided by your suppliers.
Following a risk assessment by the National Authorities of Denmark, Germany, the Netherlands, Norway and Sweden, PFAS are subject to a restriction proposal made public by ECHA on 7 February 2023. This webinar will give you a clearer picture of the content of this proposed restriction and the next steps to come.
As a food supplement supplier on Amazon, it's important to ensure that your products meet the strict regulations set by Amazon and the local laws (EU and UK regulations). Stay ahead of the game and build trust with your customers by complying with all applicable laws and guidelines. Join our webinar to successfully sell food supplement on Amazon!
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.