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.
Ingredient: SODIUM FLUORIDE
Date of publication: 12/02/2024
On February 12, 2024, the European Chemicals Agency (ECHA) announced France's intention to classify Sodium Fluoride as an endocrine disruptor for human health and reprotoxic. The restriction dossier is expected to be submitted on April 15 2025.
Topic: UK BAN ON WET WIPES CONTAINING PLASTIC
Date of publication: 07/02/2025
On February 7, 2025, Wales notified the World Trade Organization (WTO) of its intention to ban plastic-containing wet wipes, aligning with measures already adopted by England, Scotland, and Northern Ireland in the second half of 2024.
Topic: REGULATORY UPDATES
Date of publication: 01/02/2025
Several Cosmetic Regulations related to nanomaterials, vitamin A, and other ingredients will come into force from 1st February 2025, with product withdrawal deadlines later in the year.
Topic: UPDATE ON BORDERLINE MANUAL
Date of publication: 24/01/2025
On January 24, 2025, the European Commission published a revised version of the Borderline Manual that includes new criteria for determining when products in vials and ampoules qualify as cosmetics. This update provides immediate clarity for manufacturers and distributors.
Topic: EU COSMETICS REGULATION
Date of publication: 21/02/2025
On February 21 2025, the European Commission opened a Call for Evidence to assess the effectiveness of the Cosmetic Products Regulation. The revision is open for comments until March 21, 2025.
Topic: NEW REULATION ON PACKAGING MATERIALS
Date of publication: 21/02/2025
On February 21, 2025, the European Commission adopted Regulation (EU) 2025/351, introducing significant changes to existing regulations concerning plastic materials that will affect cosmetic packaging requirements.
Topic: PACKAGING AND PACKAGING WASTE
Date of publication: 22/01/2025
On January 22, 2025, the European Union (EU) Commission approved Regulation (EU) 2025/40, repealing Directive 94/62/EC. This regulation represents a major step towards sustainable packaging across different sectors, including the cosmetic industry.
Ingredient: METHYL SALICYLATE
Date of publication: 16/01/2025
On January 16, 2025, the United Kingdom notified the World Trade Organization (WTO) of an amendment to Annex III of its cosmetics regulation, introducing new restrictions on Methyl Salicylate. The UK's approach slightly differs from the EU Cosmetics Regulation.
Ingredient: SODIUM CHLORITE
Date of publication: 20/01/2025
On January 20, 2025, the European Chemicals Agency (ECHA) received a proposal from Hungary to classify Sodium Chlorite as Mutagenic 2. The proposal is open for comments until March 21 2025.
Ingredient: RESORCINOL
Date of publication: 20/01/2025
On January 20, 2025, the European Chemicals Agency (ECHA) received a proposal from France to classify Resorcinol as Endocrine Disruptor for human health. The proposal is open for comments until March 21 2025.
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.
