What is changing in the rules, what it means for your product, your municipality or your project, and who here handles it. In English and Portuguese.
Our monitoring reports record the changes to cosmetics rules in a given period, and we publish one each month. Each one is a dated publication: it reflects the rules on the date it was published and is not updated afterwards. For what applies today, read the latest briefings or ask us.
Ingredients: BENZOPHENONE, TEOPHYLLINE, PENTETIC ACID, PENTASODIUM PENTETATE
Date of publication: 08/06/2023
On 8 June 2023, the European Commission published an amendment of Annex XVII to the Regulation (EC) 1907/2006 (REACH) regarding substances recently classified as Carcinogenic, Mutagenic, or Reprotoxic (CMR). The ban is applicable from 1 december 2023.
Ingredients: METHYL-N-METHYLANTHRANILATE, HAA299 and HAA299 (nano)
Date of publication: 06/07/2023
On July 6, 2023, the United Kigndom aligned its regulation with the European Union, applying new restrictions on the ingredients Methyl-N-methylanthranilate, HAA299 and HAA299 (nano).
GREEN DOT SYMBOL - FRANCE
Date of publication: 30/06/2023
On June 30, 2023, the French Supreme Administrative Court has declared the decree issued by the French Environment Ministry regarding the Green Dot trademark to be null and void.
Ingredients: BENZYL SALICYLATE
Date of publication: 13/06/2023
On June 13, 2023, the Scientific Committee on Consumer Safety (SCCS) published the Preliminary Opinion on the safety of Benzyl Salicylate as used in cosmetic products.
Ingredients: WATER-SOLUBLE ZINC SALTS
Date of publication: 04/07/2023
On July 4, 2023, the Scientific Committee on Consumer Safety (SCCS) published the Preliminary Opinion on the safety of Water-Soluble Zinc Salts as used in cosmetic products.
Ingredients: METHYLPARABEN, BUTYLPARABEN
Date of publication: 08/06/2023
On June 8, 2023, the Scientific Committee on Consumer Safety (SCCS) published the Preliminary Opinions on the safety of Methylparaben and Butylparaben when used as preservatives in cosmetic products.
Ingredients: ALUMINIUM COMPOUNDS
Date of publication: 09/06/2023
On June 9, 2023, the European Commission requested the Scientific Committee on Consumer Safety (SCCS) to carry out an evaluation on the safety of Aluminium compounds, as used in cosmetic products.
Ingredients: ACETYLATED VETIVER OIL
Date of publication: 09/06/2023
On June 9, 2023, the European Commission requested the the Scientific Committee on Consumer Safety (SCCS) to carry out an evaluation on the inhalation toxicity of a fragrance ingredient, Acetylated Vetiver Oil (AVO), as used in sprayable cosmetic products.
Ingredients: TALC, HELIOTROPINE
On 12 June 2023, the European Chemicals Agency (ECHA) launched three consultations on proposals for harmonised classification and labelling of Talc (Carc. 2), Heliotropine (Repr. 1B) and Potassium Caroate (Skin. Corr. 1).
Ingredients: P-CYMENE, CYCLAMEN ALDEHYDE, 4-TERT-BUTYLDIHYDROCINNAMALDEHYDE
The European Chemicals Ageny (ECHA) received new harmonized classification and labelling (CLH) proposals for 3 fragrance cosmetic ingredients, which use may be at risk.
Ingredient: CYCLAMEN ALDEHYDE
Date of publication: 8 June 2026
The Scientific Committee on Consumer Safety (SCCS) has accepted a mandate to assess the safety of Cyclamen Aldehyde, following potential classification as a reproductive toxicant under the CLP Regulation.
Topic: OMNIBUS ACT IX - COSMETICS REGULATION
Date of publication: 28 July 2026
The European Commission notified the WTO about the draft Omnibus Act IX, proposing amendments to Annexes II, III, and V of the EU Cosmetics Regulation.
Topic: NEW RESTRICTIONS ON COSMETIC INGREDIENTS
Date of publication: 13 January 2026
The European Commission published Commission Regulation (EU) 2026/78, which brings new restrictions on several cosmetic ingredients that were classified as Carcinogenic, Mutagenic or Toxic for Reproduction (CMR).
Ingredient: TALC
Date of publication: January 2026
The United Kingdom (UK) Health and Safety Executive (HSE) has published a technical report concluding that Talc does not warrant carcinogenicity classification, diverging from ECHA's Risk Assessment Committee (RAC) opinion supporting Category 1B classification.
Four EUDAMED modules have been mandatory since 28 May 2026. Devices already on the market have until 27 November 2026. Who registers what, and what changed in Portugal.
From 25 February 2027, notified bodies under the MDR and IVDR must quote on defined information, keep to maximum timelines and publish their performance. What it changes for manufacturers.
Whether software is a medical device depends on what you say it is for, not on the code. The qualification test under the MDR and IVDR, updated for 2025 guidance.
Clinical data from an equivalent device can support your clinical evaluation, but the MDR sets a higher bar than the Directives did. The three characteristics, data access, and documentation.
One email when an area publishes, in the language you choose. Nothing else.
