Solution modulable pour la conformité de vos cosmétiques
Vérification de conformité de vos formules
Conformité de vos dossiers réglementaires
Solution modulable de conformité des produits
Logiciel de création & gestion des FDS
Logiciel de gestion des risques chimiques
Logiciel de traçabilité des substances à risque
Solution gratuite pour la création de FDS
Logiciel de veille réglementaire
Conformité mondiale de vos produits cosmétiques, parfums & soins
Conformité de vos produits cosmétiques aux États-Unis
Conformité de vos compléments alimentaires
Services réglementaires des substances chimiques en Europe
Accompagnement pour les dossiers d’autorisation
Enregistrement de vos substances chimiques en Europe
Veille personnalisée de la réglementation de vos substances
Conformité de vos produits Biocides
Autorisation de mise sur le marché des biocides
Approche collaborative d'AMM des produits Biocides
Suivi réglementaire des produits Biocides
Accompagnement pour vos fiches de données de sécurité
Join our exclusive webinar series to gain comprehensive insights into international cosmetic regulations. Collaborate with industry specialists to address regulatory challenges, streamline market entry, and ensure compliance across multiple regions. Enhance your understanding, stay updated on regulatory changes, and align your strategy for global success. Turn regulatory complexity into strategic advantage with EcoMundo's expertise.
Recevez une fois par mois les dernières actus réglementaires et conseils d’experts.
Unlock the complexities of North American cosmetic product regulations in our upcoming webinar. We'll dive into MoCRA, state-specific guidelines and provide strategies for efficient product registration and classification.
Discover the key regulatory requirements for cosmetic products in ASEAN and GCC countries. This webinar will offer valuable insights into regional regulations and the process of managing product registration and notifications.
Join us to explore China's regulatory landscape and e-commerce practices. Learn the essential requirements for developing cosmetic products in China. This webinar will delve into the regulations, show you how to meet these standards.
Gain a clear understanding of compliance requirements, effectively manage product classification, and stay updated with the latest regulatory changes.
If you would like to find out more about the possible consequences of the Substance’s inclusion on the Authorisation list, please join our webinar on 25 September 2024 at 11:00.
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.