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
This webinar will address the challenges related to placing PT 18 and PT 19 products on the European market, with a focus on Citriodiol.
Recevez une fois par mois les dernières actus réglementaires et conseils d’experts.
This webinar provides an in-depth overview of recent regulatory updates and upcoming environmental law obligations impacting the cosmetics industry.
Join us for a comprehensive webinar dedicated to exploring the key aspects of the REACH regulation.
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.
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