The EcoBeautyScore Consortium
The EcoBeautyScore Consortium aims to enable consumers to make sustainable choices through an environmental impact assessment and scoring system. By now, there are 36 members of the Consortium, but it remains open for other companies and associations to join.

THE ECOBEAUTYSCORE CONSORTIUM

Cosmetic and personal care companies and professional associations have come together and formed the EcoBeautyScore Consortium. So far, it is composed of 36 members from 4 continents, like Cosmetics Europe, The International Fragrance Association, L’Oréal Groupe, Shiseido, NAOS, Natrue, Unilever, Beiersdorf, and others. The Consortium remains open for other companies and associations to join, and states that it “is open to all cosmetics and personal care companies, regardless of their size or resources”.

The 36 members of the EcoBeautyScore Consortium

The Consortium is “developing an industry-wide environmental impact assessment and scoring system for cosmetics“. Its main goal is to enable consumers to make sustainable choices, providing them clear, transparent and comparable environmental impact information, based on a common science-based methodology.

The members of the Consortium are closely working with the sustainability consultancy Quantis to co-build a scientific methodology. Their work plan is based on:

  • A common method for measuring environmental impacts throughout the lifecycle of products, according to the principles of the ‘Product Environmental Footprint’ (the European Union’s PEF scientific method based on life cycle assessment (LCA) for quantifying the environmental footprint of products).
  • A common database of environmental impact of standard ingredients and raw materials used in products and packaging (including during its use).
  • A common tool that enable the assessment of the environmental impact of individual products, usable by non-experts.
  • A harmonized scoring system, which enables companies to inform consumers about the environmental footprint of their cosmetics.

The prototype is expected to be published by the end of 2022. The first step is to provide the environmental scoring for a selection of product categories, which will verified after by independent parties.

The EcoBeautyScore Consortium will consult external experts (like scientists, academics and NGOs) and its published work may be used on a strictly voluntary basis by its members and all other interested parties.

References:

  1. The EcoBeautyScore Consortium Is Now Live With 36 Industry Players In a Breakthrough Initiative to Enable More Sustainable Consumer Choices. Press Release. The EcoBeautyScore Consortium.

further
reading

cosmetic products

Citral under review: SCCS Preliminary Opinion

The SCCS was tasked by the European Commission to evaluate if the safety levels for Citral, determined through QRA2 based on skin sensitization induction, are sufficient to safeguard consumers. A preliminary opinion was released.

Read More »
cosmetic products

Are sunscreens with Benzophenone-4 safe?

Benzophenone-4 is commonly known as a UV-filter in cosmetic products. Learn what the final opinion of SCCS states about Benzophenone’s safety profile as a UV-filter in cosmetic products.

Read More »
cosmetic products

Is Aluminium in cosmetics safe for human health?

The Scientific Committee on Consumer Safety (SCCS) published its Final Opinion on the safety of Aluminium in cosmetic products. This follows a lengthy review process that began in 2013 when the SCCS was first mandated to evaluate the potential health risks of Aluminium (Al) and its compounds in cosmetics.

Read More »
cosmetic products

Silver in Cosmetics: SCCS preliminary opinion.

Ingredients: SILVER

The recent preliminary opinion from the Scientific Committee on Consumer Safety (SCCS) regarding silver in cosmetics is crucial for consumers and manufacturers. This article breaks down the key points, making it easier to understand the implications and stay informed.

Read More »
news & updates

EU Ecolabel adoption and recognition are on the rise

The Ecolabel certification is a comprehensive program focused on fostering sustainable practices. It evaluates products based on life cycle assessments, where every phase of said life cycle must abide by strict standards to attain the Ecolabel certification. The overarching objective of this certification is minimizing environmental harm from production or consumption activities.

Read More »
cosmetic products

UK proposes ban of wet wipes containing plastic 

The UK has proposed, on April 24, 2024, a regulation titled The Environmental Protection (Wet Wipes Containing Plastic) (England) Regulations 2024, to the World Trade Organization (WTO). The regulation aims to eliminate the supply and sale of plastic-containing wet wipes, including cosmetic ones. The public can offer comments on the draft until June 23, 2024, with adoption expected in September of the same year.

Read More »
news & updates

SCCS preliminary opinion on Citral sensitization endpoint

Ingredients: CITRAL

Date of publication: 27/03/2024

On March 27 2024, the Scientific Committee on Consumer Safety (SCCS) published the Preliminary Opinion on the safety of Citral in cosmetic products. The deadline for comments is set to June 2, 2024.

Read More »
medical devices

Safety Reporting in Clinical Investigations: a Gap Analysis of Guidance Documents 

Safety reporting in clinical investigations of medical devices shall be performed in line with Article 80(2) of the EU MDR. On May 2020, it was published the MDCG 2020-10/1, outlining the procedures for safety reporting in clinical investigations of medical devices under the EU MDR. However, on October 2022 the Medical Device Coordination Group (MDCG) published an updated version of the MDCG 2020-10/1, the MDCG 2020-10/1 Rev 1. This article highlights the updates included in the new revision, analysing the gaps between both documents.

Read More »
medical devices

Roles and Responsibilities of an Authorised Representative under EU MDR and IVDR 

If a medical device manufacturer is not established in a Member State, the devices can only be placed on the Union market if the manufacturer designates an authorised representative. The authorised representative plays a pivotal role in ensuring the compliance of the devices with EU regulation, serving as point of contact. The obligations and responsibilities of authorised representative are outlined on Article 11 of both MDR and IVDR, but clarification of relevant requirements is described in MDCG 2022-16 of October 2022.

Read More »
medical devices

Understanding the ISO Standards Lifecycle

ISO Standards cover a huge range of activities, representing the distilled wisdom of people with expertise in their subject matter and providing the regulators with a sound basis to develop better legislation. ISO Standards are diverse, addressing from the shoe size we wear to the quality of air we breathe. The medical device sector is no exception. ISO has many International Standards and guidance documents aimed at helping the sector ensure safe and effective medical devices while meeting the multitude of national, regional and international regulatory requirements. But how exactly is a Standard developed, reviewed and withdraw?

Read More »