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
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.
Recevez une fois par mois les dernières actus réglementaires et conseils d’experts.
The regulatory landscape for home fragrances is more complex than it may seem and is becoming increasingly challenging, particularly with the growing impact of the GPSR and environmental laws.
Lorsqu’un mélange dangereux est mis sur le marché, des obligations s'appliquent telles que la mise à disposition d’une FDS ou la déclaration au(x) centre(s) anti-poison(s). Dans cette présentation nous aborderons les notions clés à connaitre concernant la FDS et les déclarations PCN pour la mise sur le marché de vos produits en Europe !
If you missed our previous webinar, we will explore the basics of an SDS, so that you can provide your customers with the relevant information and/or control the quality of the SDSs provided by your suppliers.
EcoMundo invites you to explore regulatory and toxicological strategies to support your fragrance launches. Our goal: optimize commercial growth and ensure long-term brand sustainability through full regulatory compliance.
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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