Modular Solution for Cosmetics Compliance
Checking the Conformity of your Formulas
Compliance of your Regulatory Files
Flexible Software Solution for Product Compliance
Regulatory Monitoring Tool
Platform for the Traceability of Risky Substances
Software for Creating and Managing SDS
Software for managing your chemical risk
Worldwide Compliance for your Cosmetics, Fragrances & Skincare Products
U.S. cosmetics compliance
Compliance of your Food Supplements
Regulatory Services for Chemicals in Europe
Support for Authorization Files
Register your Chemical Substances in Europe
Customized Regulatory Monitoring of your Substances
Biocides Product Compliance
Marketing Authorization for Biocides
Collaborative Approach to Biocides Marketing Authorization
Regulatory Monitoring of Biocides
Support for your Safety Data Sheets
Recevez une fois par mois les dernières actus réglementaires et conseils d’experts.
As we conclude our Beauty Worldwide Compliance Tour: Cosmetic Regulatory Webinar Series, this final session will provide an in-depth look at sunscreen products, focusing on the challenges of formulation, classification, and registration across different regions.
Companies from the food supplements industry often have the ambition to market their products beyond the borders of their country of origin. Northen American markets have their own regulatory landscapes that both local new players and foreign exporters need to get familiar with. Whether they are named Dietary Supplements in the USA or Natural Health Products in Canada, placing such products in these territories require several regulatory steps. Through this webinar, EcoMundo will share the main guidelines for food supplements to be fully compliant when proposed to the American or Canadian consumer.
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.
In this webinar, we will first discuss the requirements applicable to e-liquids. Then, we will present an overview of the different actors in the supply chain and their obligations. We will finally walk you through the key steps for notifying mixtures and processing a PCN notification for e-liquids.
In Europe, food supplements must comply with European Directive 2002/46/EC as well as any local legislation in each country
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