Cosmetic companies obligations under REACH Regulation
REACH is a regulation of the European Union (EU) that stands for Registration, Evaluation, Authorisation and Restriction of Chemicals. All chemical substances manufactured and market in the EU, whether used in our daily lives (e.g. clothes, cleaning products, cosmetics) or industrial processes, are regulated by REACH.

REACH REGULATION 

REACH Regulation came into force on 1st June 2007 and it applies to individual chemical substances produced or imported within the European Union (EU). REACH establishes procedures for collecting and assessing information on the properties and hazards of substances. Companies must identify and manage the risk of substances they manufacture or import in the European Union (EU) to comply with this regulation.  

According to REACH, companies may have one of these roles: manufacturer, importer or downstream users. When companies are established outside the EU and export their products into the customs territory of the EU, the importer or the “only representative” of a non-EU manufacturer (both established in the EU) have the responsibility of fulfilling the requirements of REACH.  

A registration dossier, containing information on the properties, uses, hazards and potential risks of the chemical substance is submitted to the European Chemicals Agency (ECHA) by the industry. Only EU legal entities can do a REACH registration, but it is possible to do such registration using an European “Only Representative” (similar to a Responsible Person for cosmetics). Any changes to the information contained in the registration dossier must be reported immediately. For each substance, one registration must be performed, which means that if several companies work with the same substance, they must submit a joint registration.

According to REACH regulation, ECHA has the responsibility to verify if registrations are compliant. The information submitted by the companies is assessed by both ECHA and the Member States which decide if a chemical substance represents a risk to human health or the environment. Whether the substance’s risks can be managed is evaluated by ECHA’s scientific committees and Authorities. If the risks inherent to a chemical substance are considered unmanageable, authorities may ban such hazardous substances.   

REACH annexes IV and V contain substances that are exempted from registration. Annex IV to REACH regulation lists substances that are considered to cause minimum risk because of their intrinsic properties, since sufficient information is known about them (e.g. fructose; glucose; lactose). Registration is deemed inappropriate or unnecessary for the substances included in Annex V to REACH regulation. For example, substances which result from a chemical reaction that occurs incidental to storage of another substance, mixture or article, are included in Annex V. 

REACH REGULATION IMPACT ON COSMETIC PRODUCTS 

REACH impacts a wide range of companies included in several sectors. Substances used and marketed as cosmetic ingredients are within the scope of this regulation. 

In the EU, all cosmetic products are subject to Cosmetics Regulation (EC) No. 1223/2009, CLP Regulation (EC No. 1272/2008) and REACH Regulation (EC No. 1907/2006). 

When a company uses ingredients purchased from a EU supplier, it is considered a downstream user and it must check with the supplier or manufacturer of such substances if they are registered for cosmetic use or if they are exempted from registration. If, on the other hand, a company manufactures its own ingredients or imports them from outside the EU, these substances must be registered according to REACH if they are produced or manufactured above a certain threshold.  

Finished products imported from outside the EU may contain substances that are subject to REACH requirements. If a company imports these products, it is considered a REACH importer of each individual chemical substance contained in such products.  

REACH applies to new substances and also to all the existing ones. When manufacturing or importing a finished cosmetic product, which is a mixture of different substances in an article, it is necessary to register those substances under the REACH regulation. This means that finished cosmetic products are not exempted from REACH regulation obligations.

References: 

  1. Regulation (EC) No 1223/2009 of the European Parliament and of the Council of 30 November 2009, on cosmetic products. Available from: https://ec.europa.eu/health/sites/health/files/endocrine_disruptors/docs/cosmetic_1223_2009_regulation_en.pdf 
  1. Regulation (EC) No 1997/2006 of the European Parliament and of the Council of 18 December 2006 concerning the Registration, Evaluation, Authorisation and Restriction of Chemicals (REACH), establishing a European Chemicals Agency. Available from: https://eur-lex.europa.eu/legal-content/EN/TXT/PDF/?uri=CELEX:02006R1907-20140410&from=PT 
  1. European Chemicals Agency – Legislation – REACH. Available from: https://echa.europa.eu/regulations/reach/understanding-reach 

further
reading

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 »
medical devices

Amendments to the Transitional Provisions of the European Union MDR and IVDR

The proposed amendments aim to maintain patients’ access to a wide range of medical devices while ensuring the transition to the new framework. The ammendments proposal aims to extend the current transition period (Article 120 of the MDR), and it also deletes the ‘sell-off’ deadlines of both MDR and IVDR. The extension is staggered depending on the risk class of the device – until December 2027 for high-risk devices and December 2028 for medium and lower-risk devices.

Read More »
medical devices

EU MDR – Proposal for Extension of Transition Period

The transition to MDR has been slower than anticipated by the European Commission. Insufficient capacity of notified bodies and the low level of preparedness of manufacturers led to a proposal for extension of current MDR transition period with deadlines depending on the risk class of the devices.

Read More »
medical devices

MDCG 2022-18 – EU MDR Article 97

EU MDR Article 97 may be a temporary solution to avoid disruption of supply of Medical Devices on the EU Market. The MDCG 2022-18 presents a uniform approach for application of MDR Article 97 on non-compliant legacy devices under the conditions set by the competent authorities, while limiting the impact on the supply of safe and effective devices.

Read More »
parfum_fragrance_allergen_1
cosmetic products

EU to set Labelling Requirements for 56 additional Fragrance Allergens in Cosmetic Products

World Trade Organization (WTO) has been notified by the European Commission of a draft amendment to Regulation (EC) No 1223/2009 as regards labelling of fragrance allergens in Cosmetic Products. The proposed date of adoption of the new regulation is expected to be in the first half of 2023 and the propose date of entry in force 20 days from the publication in the Official Journal of the European Union.

Read More »
cosmetic products

New Amendments to the European Cosmetics Regulation – CMR Substances

The European Commission published the Commission Regulation (EU) 2022/1531, which amends Regulation (EC) No 1223/2009 in regards to the use in cosmetic products of certain substances classified as CMR. This amendment introduces new entries to Annex II and Annex III and revises an entry to Annex V to Regulation (EC) No 1223/2009.

Read More »