Cosmetic, Biocide or a Medicinal Product? An EU and US comparison
Deciding whether a product is classed as a cosmetic, biocide or medicinal product can be a complex task. Many products have dual purposes such as antibacterial hand washes and as such can fall under different regulations.
Our new whitepaper by Dr Stacey Webster aims to provide guidance on borderline products within Europe and provide a comparison to the United States with an emphasis on soaps, hand washes, cleansers and wipes.
Download the “Cosmetic, Biocide or a Medicinal Product? An EU and US Comparison” Whitepaper and other great resources here.
Learn about our new SSbD performance index, designed to predict and measure the safety of a chemistry and/or product.
Announced recently, ECHA’s enforcement authorities will initiate a project to check if duty holders have notified hazardous mixtures to poison centres in accordance with Annex VIII to CLP. Inspections will begin in January 2025 for a duration of 6 months. Learn more here.
The European Commission's recent approval of Alkyl (C12-16) Dimethylbenzyl Ammonium Chloride (ADBAC/BKC) as an active substance for use in biocidal products of product type (PT) 2 marks a significant milestone in the regulatory landscape. Learn more about this update here.
With the rapidly changing nature of the PFAS regulatory landscape, it’s important to stay on top of changes and updates. Following on from our February Q+A, here are some more key PFAS questions that our experts have answered.
Canada's Workplace Hazardous Materials Information System (WHMIS) has undergone significant revisions, aligning with the Global Harmonized System of Classification and Labelling of Chemicals (GHS) 7th revision. Learn about the updates and how to navigate the intricacies of WHMIS.
On 23 December 2023, the long-awaited amendment to the KKDIK (Turkey REACH) Regulation was published. This article provides the key takeaways from the KKDIK Amendment.
With the rapidly changing nature of the PFAS regulatory landscape, it’s important to stay on top of changes and updates. Here our Global Monitoring team answers your frequently asked questions about PFAS.
The EU Commission has recently commissioned a public consultation regarding an extension to the Biocidal Active Substance Review Programme (RP). Under the RP, any substance which was placed on the EU market as an active substance in biocidal products before 14th May 2000 must undergo an evaluation. Click to learn more.
If you're looking to market biocidal products in different regions, scoping assessment reports are a great way to evaluate your company's obligations and determine the best compliance strategy. Click for more insight into scoping assessments.
In the fast-paced world of online sales, ensuring product compliance is crucial for both businesses and consumers. With the rise of e-commerce platforms, sellers need to understand and adhere to various regulations and standards. This article delves into the importance of product compliance for online sales and provides valuable insights on how businesses can navigate this complex landscape to build trust, enhance customer satisfaction, and avoid legal complications.