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EU
Call for data on the safety Cannabidiol (CBD) used in cosmetic products
The European Commission published a call for data on the safety Cannabidiol (CBD) in the framework of Regulation (EC) No 1223/2009 with the purpose of obtaining scientific information relevant to the safety assessment of CBD in pure form and as extracts with the...
Microplastic: Upcoming EU Regulation, an open letter and the impact for cosmetic products
“Microplastic” in informal language usually refers to solid microparticles gained from synthetic polymers, typically described with a size of less than 5 mm, with a distinction made between two types depending on their origin[1]: Microparticles unintentionally formed...
Titanium dioxide – CMR classification annulled by European General Court
Titanium dioxide was classified as carcinogenic (Cat. 2), leading the European Commission to enacting Regulation (EU) 2020/217[1]. Several manufacturers and other parties such as the Titanium Dioxide Manufacturers Association (TDMA) sued against this Regulation – and...
UK
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USA
MoCRA: Draft Guidance issued by FDA – new submission portal announced for October
On 7th August 2023, the US Food and Drug Administration (FDA) issued the draft guidance on cosmetic product facility registrations and products[1], following the Modernization of Cosmetics Regulation Act (MoCRA) passed by the Congress and signed by the President as...
New regulatory requirements for cosmetic products in the United States: Consolidated Appropriations Act 2023
In the end of 2022, the omnibus spending bill passed the Congress and has been signed into law on December 29. This bill includes more than 4000 pages and also includes an amendment to the US Federal Food, Drug, and Cosmetic Act (FDCA) (sections 3501-3508)[1], often...
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