Glossary · Regulatory
The US Modernization of Cosmetics Regulation Act of 2022, which added facility registration, product listing, safety substantiation and adverse event reporting duties for cosmetics sold in the US.
Sources: 1
Missing or out-of-date regulatory work is one of the most common reasons a product is held at the border or withdrawn after launch.
Guires CSL formulation, testing, clinical and regulatory teams work with MoCRA on client projects every week, from the first brief to the final product file.
MoCRA guideRelated terms
The technical file required under Article 11 of the EU Cosmetics Regulation 1223/2009, held by the Responsible Person for ten years after the last batch is placed on the market.
Read definition →The EU online portal where every cosmetic must be notified before it is placed on the market, under Article 13 of Regulation 1223/2009..
Read definition →The legal or natural person, established in the EU (or in Great Britain for the UK), who is responsible for making sure each cosmetic complies with the regulation, holds the PIF and notifies the product..
Read definition →The ratio between a toxicological point of departure, such as a NOAEL, and the systemic exposure from using the product.
Read definition →Regulations and standards are listed first, then peer-reviewed literature. Sources checked October 2026.
Start a project
Our formulation chemists, testing scientists and regulatory specialists work alongside your team, from the first brief to a market-ready product. Bring a brief, a benchmark or just an idea: a scientist will reply within one working day with next steps and an indicative scope.