Briefings

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.

Monitoring reports, cosmetic products

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.

218 items

Results

Monitoring report

SCCS publishes preliminary Scientific Opinion on Tea Tree Oil (SCCS/1681/25)

Ingredients: Melaleuca Alternifolia Leaf Oil

Date of publication: 6 june 2025

On June 6 2025, the SCCS has published a preliminary Scientific Opinion establishing specific concentration limits for Tea Tree Oil in cosmetic products, allowing its continued use as an anti-seborrheic and anti-microbial agent despite pending CMR 1B classification under CLP Regulation.

Monitoring report

SCCS publishes Scientific Opinion on Prostaglandin Analogues (SCCS/1680/25)

Ingredients: Prostaglandin Analogues - MDN, IPCP and DDDE

Date of publication: 6 June 2025

The SCCS has concluded that none of the three prostaglandin analogues evaluated can be considered safe for use in eyelash and eyebrow cosmetic products, citing potent pharmacological activity and lack of adequate reproductive/developmental toxicity data.

Monitoring report

SCCS publishes final Scientific Advice on children’s exposure to Methyl Salicylate (SCCS/1676/25)

Ingredient: Methyl Salicylate

Date of publication: 2 May 2025

The SCCS has revised its scientific advice on children's exposure to Methyl Salicylate, establishing more restrictive concentration limits of 0.4% in toothpaste and 0.02% in other products for children aged 0-3 years, following aggregate exposure considerations from related salicylate assessments.

Monitoring report

SCCS advises on safe levels of contaminant in UV filter DHHB

Ingredient: DHHB

Date of publication: 14/02/2025

On February 14, 2025, the Scientific Committee on Consumer Safety (SCCS) adopted its scientific advice on the safety of Diethylamino Hydroxybenzoyl Hexyl Benzoate (DHHB) used as a UV-filter in cosmetic products. The deadline for comments is set to April 25, 2025.

Monitoring report

UK’s stricter BHT limits now in effect

Ingredient: BHT

Date of publication: 24/02/2025

The February 24, 2025 implementation date for the UK's new restrictions on Butylated Hydroxytoluene (BHT) has now passed, with cosmetic companies required to comply with stricter limits, particularly for oral care products.

Monitoring report

UK-wide ban on plastic-containing wet wipes to be completed with Wales joining

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.

Cosmetic Products

Monitoring report

European Commission requests SCCS Opinion on the safety of Cyclamen Aldehyde

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.

Monitoring report

European Cosmetics Regulation – Updates on Cosmetic Ingredients  

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).

Monitoring report

United Kingdom publishes Technical Report on the Classification and Labelling of Talc 

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.

Medical Devices

EU

How to demonstrate equivalence under the MDR

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.

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