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In 2025, the UK Government launched a public consultation on extending the UK REACH registration deadlines and presented several options for consideration. In December, a summary report was published, confirming that the first option had been selected and that the amendment would officially enter into force in 2026. Within this context, The REACH (Amendment) (No. 2) Regulations, which bring the relevant amendment into effect, were officially published in July 2026. What Are the New Deadlines? The relevant Regulations will officially enter into force on 6 August 2026. From that date onwards, the following deadlines will apply: Tonnage Band Transitional Registration Deadline All substances manufactured or imported at ≥1,000 tonnes per year Substances very toxic to aquatic organisms manufactured or imported at ≥100 tonnes per year CMR substances manufactured or imported at ≥1 tonne per year Substances included in the EU SVHC List before 31 December 2020 27 October 2029 All substances manufactured or imported at ≥100 tonnes per year Substances added to the UK SVHC List before October 2029 27 October 2030 All substances manufactured or imported at ≥1 tonne per year 27 October 2031 Other Amendments Introduced by the Regulations The period applicable to Protected Transitional Imports (PTI) has been extended in line with the updated UK REACH registration timetable. The deadlines for HSE compliance checks have also been updated in accordance with the new registration timetable, according to article 41(5): 27 October 2030: First registration phase 27 October 2032: Second registration phase 27 October 2036: Final registration phase The 2026 Regulations only extend the registration deadlines. The Alternative Transitional Registration Model (ATRm) has not yet entered into force. Chemleg Can Help Chemleg can help you prepare for the applicable deadlines through its UK REACH registration services. Complete the form below to arrange a meeting with our experts.

The UK Health and Safety Executive (HSE) announced that the UK REACH SVHC Candidate List was updated on 15 June 2026. Within this scope, the following 15 substance groups have been added to the list. 2,2′,6,6′-Tetrabromo-4,4′-isopropylidenediphenol (TBBPA) 2,2-Bis(bromomethyl)propane-1,3-diol (BMP); 2,2-dimethylpropan-1-ol tribromo derivative/3-bromo-2,2-bis(bromomethyl)-1-propanol (TBNPA); 2,3-dibromo-1-propanol (2,3-DBPA) 2-(4-tert-Butylbenzyl)propionaldehyde and its individual stereoisomers (Lysmeral) 2-(Dimethylamino)-2-[(4-methylphenyl)methyl]-1-[4-(morpholin-4-yl)phenyl]butan-1-one (Omnirad) 6,6′-Di-tert-butyl-2,2′-methylenedi-p-cresol (DBMC) 6-[(C10-C13)-alkyl-(branched, unsaturated)-2,5-dioxopyrrolidin-1-yl]hexanoic acid (Tetra-PSCA) Barium diboron tetraoxide Bis(2-(2-methoxyethoxy)ethyl) ether (tetraglyme) Bis(α,α-dimethylbenzyl) peroxide Dioctyltin dilaurate, dioctyltin bis(cocoacyloxy) derivatives, and other dioctyltin bis(fatty acyloxy) derivatives (DOTL) Diphenyl(2,4,6-trimethylbenzoyl)phosphine oxide N-(Hydroxymethyl)acrylamide Orthoboric acid, sodium salts Reactive Brown 51 Tris(2-methoxyethoxy)vinylsilane This new decision was taken following the public consultation process launched by the HSE on 9 March 2026. After the process ended on 20 April, the substances concerned were identified as SVHCs and added to the Candidate List. Click here to review the updated Candidate List. The HSE has also announced that further consultations will be carried out for additional SVHC substances. Companies are advised to follow the HSE e-bulletin. What Are the Obligations Relating to These Substances? Under UK legislation, companies must fulfil certain information and notification requirements where substances included in the Candidate List are present in the products they supply. Where a substance included in the Candidate List is present in an article at a concentration above 0.1% (w/w), the necessary information for the safe use of the article must be provided to the recipient. Where articles containing substances included in the Candidate List are produced, imported or placed on the market, a notification to the HSE may be required if certain conditions are met. In addition, information obligations also apply to mixtures that are not classified as hazardous under the GB CLP Regulation but contain a Candidate List substance. Where a mixture contains a Candidate List substance at a concentration of 0.1% or above, a safety data sheet (SDS) must be provided upon request. Furthermore, where a substance placed on the market is included in the UK REACH Candidate List, the supplier is required to provide the customer with the safety data sheet for the relevant substance. These obligations aim to ensure that Candidate List substances are managed transparently throughout the supply chain and that safe use information is communicated to the relevant parties. Contact Us and Let Us Review Your Portfolio Together Chemleg can support you in ensuring your UK REACH compliance. You can click here to obtain information about our services and complete the form to speak with our experts.

ECHA’s Enforcement Forum has defined the scope of new EU-wide enforcement projects to be carried out in the coming years. According to the decisions, inspections will focus on areas such as restricted hazardous substances in products, tattoo inks and permanent makeup, CLP implementation and the online sale of biocidal products. Restricted Substances in Products to Be Inspected Under REF-16, inspectors will check whether products and mixtures placed on the market comply with restrictions under EU chemicals legislation. The inspections will particularly examine whether: In cooperation with the European Commission and National authorities, it will also be assessed how findings obtained from online sales can support enforcement activities under the Digital Services Act. . Inspections are planned for 2028, with the report expected in 2029. Pilot Project on Tattoo Inks and Permanent Make-up Products The Forum has also decided to launch a new pilot project on tattoo inks and permanent make-up products. Under this project, inspectors will check whether: Inspections are planned to start in 2027, and the report will be published in 2028. Rapid Enforcement Initiative on CLP Obligations The Forum has also launched its first Rapid Enforcement Initiative (REI-1). Within the scope of this initiative: Online Sales of Biocidal Products Under Scrutiny The Forum’s Biocidal Products Regulation Subgroup (BPRS) has announced that the next EU-wide biocidal products enforcement project (BEF-4) will focus on online sales and cross-border cooperation. The inspections will particularly check whether online advertisements for biocidal products such as wood preservatives, rodenticides and insecticides comply with information requirements. In addition, the inspections will check whether: Inspections are planned for 2028, with the report expected in 2029. What Can You Do? Although the inspections are planned to start in 2028, it would be beneficial for companies whose products may fall within this scope to begin preparations now. In this context, companies should review their product portfolios and determine whether their products contain substances restricted under EU legislation. They are required to have comprehensive technical documentation to demonstrate compliance during inspections. Companies should also ensure that product descriptions, label information and legal warnings are complete. Attention should also be paid to compliance with product-type-specific requirements. These preparations will significantly reduce the risk of non-compliance during possible inspections. You can benefit from Chemleg services to ensure full compliance with the regulations. Fill in the form to arrange a meeting with our experts.

What is the Chesar Platform? The Chesar Platform is a tool that will help companies complete and report their chemical risk assessments under REACH and the Biocidal Products Regulation. It is accessible via ECHA Cloud Services. What is the Chesar Platform used for? The Chesar Platform brings chemical risk assessment processes together in a single modern, integrated environment. With this tool: Risk assessments can be carried out in a more organised and structured manner. Exposure estimation tools can be used as integrated tools within the platform. Reporting processes are made more consistent. Updates made during assessments can be managed more easily. Calculations can be automatically refreshed and reports can be regenerated. REACH users can use the platform when preparing chemical safety assessments, generating Chemical Safety Reports, or preparing the exposure scenarios included in safety data sheets. Biocidal product users can use it when carrying out environmental exposure and risk assessments for substances and when preparing the Risk Assessment Report / Competent Authority Report sections for active substances. ECHA recommends that users start the transition process to the new platform and review the platform’s user manual, release notes and migration guides. ECHA has also noted that the previous Chesar 3 tool will continue to be supported for approximately one more year. Webinar resources prepared by ECHA on the main features of the Chesar Platform and how to get started with its use have also been made available to users. You can click here to access the Chesar Platform. You can obtain detailed information on the subject by watching ECHA’s relevant webinar.

As of July 2026, ECHA will start publishing the names of companies that have submitted notifications to the Classification and Labelling (C&L) Inventory. Companies wishing to keep their company names confidential must submit a request by 30 June 2026. The information provided by ECHA on this matter can be summarised as follows: Company names will be published in the C&L section of ECHA CHEM and will be made available in separate lists for each classification and substance type. At the initial stage, it is planned that only the names of companies linked to CLP notifications will be published. In the case of group notifications, the name of the company acting on behalf of the group will be published, while the names of the members will not be published. For Classification and Labelling (C&L) information originating from REACH registrations, the registrant information already available in the Dossier section of ECHA CHEM will be displayed in the C&L Inventory. According to ECHA, this change follows the 2024 revision of the Classification, Labelling and Packaging (CLP) Regulation and aims to help companies reach agreement on classification and labelling entries for the same substance. Do You Not Want Your Company Name to Be Published? Companies with a valid justification for keeping their names confidential must submit an updated notification including a confidentiality request before the deadline of 30 June 2026. A video explaining the relevant steps has been published. You can access it by clicking here. Fill out the form and contact us for support regarding your CLP notifications.

According to the European Chemicals Agency (ECHA), the Biocidal Products Committee (BPC) adopted six opinions concerning active substances and two opinions concerning Union authorisations during its meeting held on 23–25 February 2026. The details of these opinions are as follows: Opinions adopted regarding active substances   Approval for use of ethanol in Product types 1, 2 and 4 (You can access further details on the topic here).Non-approval for use of DMDMH in Product types 6 and 13.Support for the renewal of hydrochloric acid for Product type 2. Opinions adopted regarding Union authorisation Authorisation of a biocidal product family containing C(M)IT/MIT (3:1) for Product types 6, 11, 12 and 13.Authorisation of a biocidal product family containing peracetic acid for Product type 3. ECHA has announced that the next BPC meeting will take place on 25–29 May 2026. For further details regarding the opinions, you may review ECHA’s article. Learn Your Obligations You may contact us to learn about your obligations regarding the use of active substances and Union authorisation for biocidal products and to ensure compliance with the relevant legislation. To schedule a meeting with our experts, please fill out the form.

On 6 January 2026, an announcement was published on the website of the Ministry of Environment, Urbanisation and Climate Change of the Republic of Türkiye. In this announcement, the deadline for companies to complete their KKDIK individual temporary registration processes was specified, and guidance was provided to companies. KKDIK Individual Temporary Registration Process KKDIK individual temporary registration is a method that allows companies to complete temporary registration procedures without the presence of a Lead Registrant. According to the announcement, regardless of whether a Lead Registrant exists and regardless of the tonnage band, all substances within the scope of KKDIK must have either a temporary registration or a full registration by 30 September 2026. The application types that can be completed by this date are joint submission full registration, joint submission temporary registration, and individual submission temporary registration. The Ministry has also published the KKDIK Individual Temporary Registration Flowchart to guide companies in this process. Click here to read the English translation of the announcement. Complete Your KKDIK Processes with Chemleg Since its establishment, Chemleg has supported numerous companies in KKDIK processes and has helped them maintain their presence in the Turkish market with confidence. To learn more about our KKDIK registration services, you may review our service page and fill out the form so that our experts can contact you.

On 2 March 2026, Regulation (EU) 2026/405 of the European Parliament and of the Council on detergents and surfactants was published in the Official Journal of the European Union. This Regulation repeals the former Regulation (EC) No 648/2004, making a new era for the detergent products industry. Entry into Force and Application Dates The Regulation will enter into force on 22 March 2026. To allow the industry sufficient time to adapt to these transformative changes, a transitional period has been established: most provisions will become mandatory starting 23 September 2029. What Does the New Regulation Include? The new regulatory framework introduces several key changes, particularly aligned with the Union’s green and digital transition objectives. You can examine the full text of the Regulation here: Regulation (EU) 2026/405 – EUR-Lex. What Should Companies Do? Companies are advised to begin assessing the impact of this Regulation immediately and utilize the transitional period wisely. It is recommended that firms start reviewing their product formulations, evaluating labelling obligations, and preparing their digital compliance systems (such as the DPP infrastructure). Chemleg is ready to assist you throughout this process. You can fill out the form to schedule a meeting with our experts.

The Biocidal Products Committee (BPC) of the European Chemicals Agency (ECHA) held a meeting in February. During the meeting, the use of ethanol as an active substance was approved for the following product types: The use of ethanol within these product types was supported by the Biocidal Products Committee. For ethanol in these uses, no new hazard classification was proposed. Therefore, it has been concluded that the safe use of ethanol has been demonstrated for these product types. What Happens Next? Following the Biocidal Products Committee’s opinion, ECHA will submit it to the European Commission in the coming days for the adoption of a final decision. The Commission will prepare a regulation concerning the final decision and submit it to the EU Member States for vote by the competent authorities. If the Commission formally adopts the decision, it will become legally binding. If the decision is approved, biocidal products containing ethanol may be authorised authorisation under the Biocidal Products Regulation. In such a case, companies will be required to apply either for Union authorisation or for product authorisation at national level. If the decision is not approved, products containing the substance must be withdrawn from the EU market within the applicable transitional period, as stated by ECHA. You may access ECHA’s related news by clicking here. This article was originated from ECHA. Contact Chemleg Chemleg is ready to answer all your questions regarding your biocidal products. Please fill out the form to benefit from our consultancy services.

With the latest additions, the number of substances of very high concern (SVHCs) on the Candidate List has increased to 253. The new chemicals added to the Candidate List on 4 February 2026 were announced by ECHA as follows: These substances may be included in the Authorisation List in the future. In such a case, companies will be required to apply for authorisation in order to continue using these substances. Click here to access the updated Candidate List. What Should Companies Do? ECHA has outlined the obligations of companies as follows: This article was originated from ECHA. Contact Chemleg For any questions regarding this matter, please complete the form below.

The Turkey REACH – KKDIK fees to be charged by the Ministry of Environment, Urbanization and Climate Change of the Republic of Türkiye for 2026 have been announced. The updated fees are published in the “2026 Unit Price List” available on the website of the Revolving Fund Management Directorate. What Are the New KKDIK Fees? Required fees for registration under Articles 7, 8 and 12 of KKDIK Regulation Article 7: General registration obligation for substances as such or in a mixture Article 8: Registration of substances in articles Article 12: Joint submission of data by more than one registrant Table 1: Standart fees   Individual Submission (TRY) Joint Submission (TRY) Fee for substances between 1-10 tonnes 6412 4881 Fee for substances between 10-100 tonnes 16075 11294 Fee for substances between 100-1000 tonnes 45151 32514 Fee for substances more than 1000 tonnes 96990 77665   Table 2: Reduced fees for SMEs   Medium-sized Enterprise (Individual submission) (TRY) Medium-sized Enterprise (Joint submission) (TRY) Small-sized Enterprise (Individual submission) (TRY) Small-sized Enterprise (Joint submission) (TRY) Micro-sized Enterprise (Individual submission) (TRY) Micro-sized Enterprise (Joint submission) (TRY) Fee for substances between 1-10 tonnes 3250 1982 1631 991 627 326 Fee for substances between 10-100 tonnes 9662 5872 4881 2974 1280 627 Fee for substances between 100-1000 tonnes 25650 12825 9662 6412 2622 991 Fee for substances more than 1000 tonnes 65016 32514 27457 18246 6412 3250 Fees to be paid for registration under Article 17(2), Article 18(2) and (3) or Article 19 of KKDIK Regulation Article 17: Registration of on-site isolated intermediates Article 18: Registration of transported isolated intermediates Article 19: Joint submission of data on isolated intermediates by more than one registrant Table 1: Standart fees   Individual Submission (TRY) Joint Submission (TRY) Fee 6412 4693   Table 2: Reduced fees for SMEs   Medium-sized Enterprise (Individual submission) (TRY) Medium-sized Enterprise (Joint submission) (TRY) Small-sized Enterprise (Individual submission) (TRY) Small-sized Enterprise (Joint submission) (TRY) Micro-sized Enterprise (Individual submission) (TRY) Micro-sized Enterprise (Joint submission) (TRY) Fee 3250 1982 1631 991 627 326   Required fees for registration update under Article 22 of KKDIK Regulation Article 22: Other duties of the registrant Table 1: Standard fees for tonnage band update   Individual submission (TRY) Joint submission (TRY) From 1-10 tonnage band to 10-100 tonnage band 9662 6412 From 1-10 tonnage band to 100-1000 tonnage band 38826 27457 From 1-10 tonnage band to more than 1000 tonnage band 90315 72784 From 10-100 tonnage band to 100-1000 tonnage band 29364 20956 From 10-100 tonnage band to more than 1000 tonnage band 81279 66108 From 100-1000 tonnage band to more than 1000 tonnage band 52379 45151   Table 2: Reduced Fees for SMEs for tonnage band update   Medium-sized Enterprise (Individual submission) (TRY) Medium-sized Enterprise (Joint submission) (TRY) Small-sized Enterprise (Individual submission) (TRY) Small-sized Enterprise (Joint submission) (TRY) Micro-sized Enterprise (Individual submission) (TRY) Micro-sized Enterprise (Joint submission) (TRY) From 1-10 tonnage band to 10-100 tonnage band 6412 3978 3250 1982 627 326 From 1-10 tonnage band to100-1000 tonnage band 22575 10842 7855 5421 1982 627 From 1-10 tonnage band to more than 1000 tonnage band 61414 30343 25650 18421 5872 2974 From 10-100 tonnage band to 100-1000 tonnage band 16075 7039 4693 3614 1631 326 From 10-100 tonnage band to more than 1000  tonnage band 55090 26553 22575 16439 5421 2622 From 100-1000 tonnage band to more than 1000 tonnage band 38839 18246 18058 12825 3789 2258 Table 3: Fees for other updates Update Type Change in the registrant’s identity including a change in legal entity 4693 Update Type Individual submission (TRY) Joint submission (TRY) Change in information access permission in the submission Change in purity and/or identity of impurities or additives 12825 9662 Relevant tonnage band 4693 2258 A study summary or comprehensive study summary 12825 9662 Information in the safety data sheet 9662 6412 Trade name of the substance 4693 2258 IUPAC name for substances referred to in Article 61(1)(a) of KKDIK Regulation* 4693 2258 * Electronic public access   Table 4: Reduced Fees for SMEs for other updates Update Type Medium Enterprise (TRY) Small Enterprise (TRY) Micro Enterprise (TRY) Change in the registrant’s identity including a change in legal entity 3250 1631 326 Update Type Medium-sized Enterprise (Individual submission) (TRY) Medium-sized Enterprise (Joint submission) (TRY) Small-sized Enterprise (Individual submission) (TRY) Small-sized Enterprise (Joint submission) (TRY) Micro-sized Enterprise (Individual submission) (TRY) Micro-sized Enterprise (Joint submission) (TRY) Change in information access permission in the submission Change in purity and/ or identity of impurities or additives 9662 6412 5057 3250 1280 991 Relevant tonnage band 3250 2258 1631 991 464 326 A study summary or comprehensive study summary 9662 6412 5057 3250 1280 991 Information in the safety data sheet 4693 3250 2622 1982 991 627 Trade name of the substance 3250 2258 1631 991 464 326 IUPAC name for substances referred to in Article 61(1)(a) of KKDIK Regulation 3250 2258 1631 991 464 326 Required fees for submissions under Item (11) of Article 11(1)(a) in KKDIK Regulation Article 11 (1) (a) 11: The request of the manufacturer or importer on not to disclose information on the internet in accordance with the second paragraph of Article 61 and its justification by explaining why publishing would be hazardous for the commercial interests of the person or another related party. – Non-public access information request Table 1: Standart fees Requested confidentiality Individual submission (TRY) Joint submission (TRY) The degree of purity and/or identity of impurities or additives 12825 9662 Relevant tonnage band 4693 2258 A study summary or comprehensive study summary 12825 9662 Information in the safety data sheet 9662 6412 Trade name of the substance 4693 2258 IUPAC name for substances referred to in Article 61(1)(a) of KKDIK Regulation* 4693 2258   Table 2: Reduced Fee for SMEs Requested confidentiality Medium Enterprise (Individual submission) (TRY) Medium Enterprise (Joint submission) (TRY) Small Enterprise (Individual submission) (TRY) Small Enterprise (Joint submission) (TRY) Micro Enterprise (Individual submission) (TRY) Micro Enterprise (Joint submission) (TRY) The degree of purity and/or identity of impurities or additives

With Commission Regulation (EU) 2025/2573 dated 18 December 2025, the test methods applicable under the REACH Regulation have been updated. Under this amendment: Human Health, Ecotoxicity, and Nanoforms Structural and Technical Amendments To improve efficiency, additional explanatory notes for certain test methods have been removed. Instead, the updated tables in Part 0 and references to international standards have been adopted as the basis. Updates and Additions Six new OECD test guidelines have been introduced, as listed below: The following test guidelines have been updated: In addition, Commission Regulation (EU) 2025/2573 introduces four new test methods related to the dustiness endpoint (for nanoforms of a substance): Furthermore, A.13 (Pyrophoric Solids and Liquids) in Part A, B.2 (Acute Inhalation Toxicity) in Part B, and B.70 (Estrogen Receptor Binding Assay) in Part B have been deleted. Date of Entry into Force The Regulation will enter into force in all EU Member States on 8 January 2026. For further information and support, you may contact us by completing the form below.

On 26 November 2025, the European Parliament and the Council formally adopted Regulation (EU) 2025/2439. This Regulation introduces critical amendments to Regulation (EU) 2024/2865, specifically regarding the dates of application and transitional provisions. The primary objective of this postponement is to reduce administrative burdens and simplify implementation for companies, aligned with the findings of the 2024 Draghi Report on European competitiveness. The Commission identified that certain requirements, such as those for fuel dispensers at filling stations, were impractical and costly without providing significant health or environmental benefits. New Application Timeline Based on the updated Regulation, the new application dates for the various provisions are as follows: Application Date Provisions and Requirements 1 July 2026 Formatting of labels (Article 1(17)), refill stations (Article 1(18)), specific concentration limits and M-factors (Article 1(22)), and specific sections of Annex I and II. 1 January 2027 Information requirements for poison centres (Article 1(9)), Member State responsibilities (Article 1(24)), and Annex IV. 1 January 2028 Information requirements for advertisements (Article 1(14)), distance sales offers (Article 1(15)(c)), and relabelling requirements (Article 1(26) and (27)). Transitional Provisions (Voluntary Application) To ensure legal clarity, economic operators are permitted to apply the new rules on a voluntary basis before the mandatory deadlines. The derogation periods are structured as follows: Provisions of Regulation (EU) 2024/2865 that are not related to formatting or administrative burdens, and which ensure a high level of protection for human health and the environment, remain unchanged in their original application schedule. This Regulation shall enter into force on the twentieth day following its publication in the Official Journal. Any questions? For detailed information and support on this matter, please submit the form below.

As you may already know, the UK Department for Environment, Food & Rural Affairs (DEFRA) opened a public consultation on 14 July 2025, which remained open until 8 September 2025. On 22 December 2025, DEFRA published the outcome of the consultation on its official website. Accordingly, the government has decided to proceed with the dates set out as Option 1 in the consultation. It stated that the additional time provided under Option 1 will help reduce the burden on small and micro-enterprises and downstream users. At the same time, this approach will ensure that data are available at an appropriate point in time. As stated in the official announcement, the UK government intends, subject to the consent of the Scottish and Welsh Ministers, to bring forward legislation extending the UK REACH submission deadlines to the dates specified under Option 1. The new UK REACH deadlines are as follows: Deadline Tonnage 27 October 2029 1,000 tonnes or more per year 27 October 2030 100 tonnes or more per year 27 October 2031 1 tonne or more per year According to the announcement, the government also intends, subject to the consent of the Scottish and Welsh Ministers, to legislate to align the statutory compliance check dates under Article 41(5) with the new submission deadlines. The new legislation will be brought forward in 2026 following the ordinary parliamentary procedure, ensuring that the revised deadlines and compliance arrangements enter into force in good time before the first extended deadline in October 2029. To access the official announcement, please click here. For updates on UK REACH, you may follow us on our LinkedIn account, or complete the form below to receive support from our team.

At its meeting in November, ECHA’s Biocidal Products Committee (BPC) adopted four opinions on active substances and three opinions on Union authorisations. Opinions Adopted on Active Substances Opinions Adopted on Union Authorisations Biocidal products or biocidal product families must be authorised by the European Commission in order to be made available on the market and used within the European Union and the  European Economic Area. In this context, the biocidal product families for which a Union authorisation opinion was adopted in November are as follows: Opinions Adopted on Post-Authorisation Data What Should Companies Do? The European Commission, together with the EU Member States, will take the final decisions on these opinions. Please stay tuned for updates. Further information on the Committee’s decisions is available on ECHA’s website. Click here to reach.

The European Chemicals Agency (ECHA) has introduced a new tool called B-Risk to facilitate the assessment of risks that biocidal products may pose to bees. The tool is aligned with ECHA’s 2024 Bee Guidance, which will apply as of February 2026. It should be noted that this will not apply to active substances in the review programme. According to ECHA, B-Risk was developed in line with the “one substance, one assessment” approach. It is essentially an extension of the European Food Safety Authority (EFSA), originally designed for plant protection products, but adapted to meet the specific requirements of biocidal products, particularly insecticides. What Does B-Risk Do? With B-Risk, users can carry out the environmental risk assessments required under the Biocidal Products Regulation (BPR). The tool is particularly valued for its contribution to protecting bee health and supporting the EU’s biodiversity goals. Key features of B-Risk for biocides include: How Can You Access B-Risk? B-Risk is accessible via ECHA’s Support page. From there, users are directed to EFSA’s R4EU platform, where the tool is hosted. B-Risk operates entirely online. To access it, users must register on R4EU and accept EFSA’s terms of use. Click here to access the original source and learn more.

As you may know, the EU-wide restriction on microplastics, which entered into force in October 2023, prohibits the intentional use of microplastics in products such as cosmetics, detergents, and certain agricultural products, as well as in some processes where these microplastics are released into the environment. According to ECHA, the Regulation introduces reporting obligations for manufacturers, importers, downstream users, and suppliers placing SPMs or products containing SPMs on the market for certain exempted uses, with the aim of helping monitor and reduce microplastic emissions. Reporting Process for SPMs Has Opened In an article published on its website, ECHA announced that companies can now begin reporting their annual releases under the microplastics restriction. This obligation applies to exempted uses of synthetic polymer microparticles (SPMs), and the deadlines for submitting reports are specified as follows: for manufacturers and industrial downstream users of SPMs in the form of pellets, flakes and powders, used as raw material in plastic production at industrial sites; and 31 May 2026 for all other manufacturers and industrial downstream users of SPMs at industrial sites, as well as for suppliers placing products containing SPMs on the market for the first time for specific exempted uses by professionals or the public   31 May 2027 ECHA notes that examples of exempted SPM uses include veterinary and human medicinal products, food additives, in vitro diagnostic devices, and certain uses at industrial sites. Who is subject to the obligation? The obligation applies to manufacturers, importers, and downstream users alike. In addition, suppliers of SPMs and products containing SPMs are subject to the requirements under certain conditions, particularly when placing such products on the market for the first time. How should the reports be prepared? Companies must prepare annual release reports in IUCLID format and submit them to ECHA via REACH-IT. It should be noted that for now, only initial submissions are possible in REACH-IT. Updates will be allowed from Q2 2026. During this process, companies may use ECHA’s guidance and informational materials, as well as the IUCLID dataset prepared to support users. Click here to access the relevant documents and the source of the news.

On 5 November 2025, the following substance was added to the Candidate List of Substances of Very High Concern (SVHC): Substance name 1,1′-(ethane-1,2-diyl)bispentabromobenzene (DBDPE) EC number 284-366-9 CAS number 84852-53-9 Reason for inclusion Very Persistent and Very Bioaccumulative, vPvB (Article 57e) Example uses Flame retardant Substances added to the Candidate List may also be included in the Authorisation List in the future. If a substance appears on this list, companies can only continue using it after applying for and obtaining authorisation from the European Commission. What should companies do? According to the European Chemicals Agency (ECHA), the following obligations apply to companies: Click here to reach the Candidate List. For more information and to benefit from our registration services, you may fill out the form below:

The European Commission has adopted a revised REACH Fee Regulation, introducing significant changes to chemical registration and authorisation procedures. The new regulation includes innovations such as a mandatory pre-verification for SMEs and increased fees for large companies. The regulation will enter into force 20 days after its publication in the Official Journal of the EU. The ex-ante verification system will become applicable 15 months after the entry into force. Until that date, the current SME verification procedure will remain valid. Fee Increase According to the revised REACH Fee Regulation, standard fees and charges for large companies will increase by 19.5%. This increase is based on the average annual inflation rate in Europe for 2021–2023 and applies only to large enterprises to preserve the competitiveness of SMEs. The updated fees will take effect on 5 November 2025. While reflecting overall economic conditions, the fee increase also aims to reduce the financial burden on smaller businesses. This approach maintains SMEs’ market position while increasing the expected contribution rate from large companies. New Requirements for SMEs Starting from 5 February 2027: The new pre-verification system will clarify a company’s status in advance, simplifying ECHA’s evaluation process and reducing administrative burdens caused by incorrect declarations. Validity and Renewal of SME Status This system eliminates the need for SMEs to submit extensive documentation for each application, saving both time and costs. To facilitate the transition to the new system, ECHA will gradually publish guidance documents to support companies in preparing for the SME verification process. These guides are expected to provide practical information on required documentation, timelines, and common mistakes.  You can review the REACH Fee Regulation here. Fill out the form to start preparing your documentation. Related Services REACH Registration Product Stewardship Only Representation

On 22 October 2025, a draft titled “On Amendments to the Resolutions of the Cabinet of Ministers of Ukraine of May 10, 2024, No. 539 and of July 23, 2024, No. 847” was published. In the draft that is published by Ministry of Economy, Environment and Agriculture (MEEA) the amendments primarily extend timelines to align with the phased for giving industry additional time for dossier preparation and labelling updates. Please note that these amendments are still draft and not in force. The main amendments introduced by this draft regulation are as follows: Process Previous Deadline Updated Deadline UA REACH Pre-registration Deadline 26 January 2026 26 January 2027 UA REACH Registration Deadlines     Substances classified as CMR (Cat. 1A and Cat. 1B) in quantities of ≥ 1 ton/year Substances classified as H400 and H410 (Cat. 1) in quantities of ≥ 100 ton/year 26 January 2026 1 October 2028 Substances manufactured or imported ≥ 1000 tonnes/year 1 October 2026 1 October 2029 Substances manufactured or imported between 100–1000 tonnes/year 1 June 2028 1 June 2031 Substances manufactured or imported between 1–100 tonnes/year 1 March 2030 1 March 2033 Please note that in this draft, A six-month extension could be assumed for C&L Notification, potentially indicating a new deadline around 15 May 2026. Since the currently in-force deadline remains 15 November 2025, preparing a C&L Notification in advance would be an important step to ensure regulatory compliance and market safety. The draft has been published on the official website of the Ministry of Economy, Environment and Agriculture of Ukraine for public consultation, and the approval process of the decree has not yet been finalized. Click here to access the official announcement and share your comments on the draft. Don’t forget to subscribe to our newsletter for future updates on the subject. You can review the related documents through the links below: Related Services Only Representation UA REACH Pre-registration UA C&L Notification

On 3 October 2025, the European Commission adopted new measures restricting the use of PFAS in firefighting foams. PFAS use is one of the major sources of environmental pollution in the European Union. To protect human health and the environment, the Commission introduced new measures to restrict the use of PFAS (per- and polyfluoroalkyl substances) under the REACH Regulation. This restriction aims to minimise PFAS emissions and prevent the release of approximately 470 tonnes of PFAS into the environment each year. According to the Commission’s announcement, this measure will help reduce soil and water contamination while also protecting firefighters from exposure to PFAS-containing foams. Based on the scientific assessment of the European Chemicals Agency’s (ECHA) committees, the restriction includes specific transition periods to allow industry to switch to PFAS-free alternatives, which are stated in the related Regulation. The new regulation will officially enter into force 20 days after its publication in the Official Journal of the European Union. It will become applicable following transition periods ranging from 12 months to 10 years, depending on the use, providing sufficient time for the replacement with safer and more effective alternatives. You can review the Comission Regulation (EU) 2025/1988 below. Click here to access the official source of the news.

At its September meeting, which took place on 9–11 September 2025, the Biocidal Products Committee (BPC) of the European Chemicals Agency (ECHA) adopted four opinions on active substances and six on Union authorisations. Adopted Opinions on Active Substances Regarding carbon dioxide, ECHA made the following statement: “Supporting the amendment of the inclusion of Carbon dioxide (CO₂) in Annex I of the Biocidal Products Regulation (BPR). This inclusion in Annex I is restricted to: ‘Only for use in ready-for-use gas canisters functioning together with a trapping device.’” At the meeting, a request was made to revise the existing restrictions on CO₂, upon which the BPC proposed the following: “For product authorisations it shall be ensured that the exposure for professional users remains below the acceptable exposure concentration (AEC): 1.5% v/v carbon dioxide for the STEL (short-term exposure limit) 15 minutes, and 0.5% v/v carbon dioxide for the TWA (time-weighted average) 8 hour.” ECHA stated that this new restriction would enable broader authorisation of CO₂-based products while ensuring safe use within the defined exposure limits. Non-approval of Poly(dimethyloctadecyl[3-(trihydroxysilyl)propyl]ammonium chloride) Poly(dimethyloctadecyl[3-(trihydroxysilyl)propyl]ammonium chloride) generated from di-methyloctadecyl[3-(trimethoxysilyl)propyl]ammonium chloride (DMOAP)was proposed for use in the following product-types: Product-type 2 – Disinfectants and algaecides not intended for direct application to humans or animals, Product-type 7 – Film preservatives, Product-type 9 – Fibre, leather, rubber and polymerised materials preservatives. However, the BPC recommended non-approval for all three product types, as no safe use was identified. Six Union Authorisations Supported At the September BPC meeting, the following Union authorisations were supported: A biocidal product containing active chlorine generated from sodium chloride by electrolysis for product-types 2 and 4 (food and feed area); A biocidal product containing Alkyl (C12–16) dimethylbenzyl ammonium chloride (ADBAC/BKC (C12–16)) and Glutaral (Glutaraldehyde) for product-types 3 (veterinary hygiene) and 4; A biocidal product containing Peracetic acid for product-type 2; A biocidal product family containing L-(+)-lactic acid for product-types 2 and 4; A biocidal product family containing Peracetic acid for product-types 2, 3 and 4; and A biocidal product family containing Glutaral (Glutaraldehyde) for product-types 6, 11 and 12. Decisions and Competent Authorities The ECHA annex provides information on Commission decisions and competent authorities. These are summarised in the table below: Topic Product-Types Decision Rapporteur Member State Opinion on approval of DMOAP 2, 7, 9 Not approved Spain CO₂ Annex I inclusion – Approved Netherlands Biocidal product containing active chlorine generated from sodium chloride by electrolysis 2, 4 Approved (simple majority) France Biocidal product containing ADBAC/BKC and Glutaraldehyde 3, 4 Approved Belgium Biocidal product containing Peracetic acid 2 Approved Germany Biocidal product family containing L-(+)-lactic acid 2, 4 Approved Germany Biocidal product family containing Peracetic acid 2, 3, 4 Approved (simple majority) Netherlands Biocidal product family containing Glutaraldehyde 6, 11, 12 Approved Netherlands Questions on the risks of exposure of workers to corrosive particles during the use of biocidal products by coarse spraying – Approved France and Belgium Examination of alternatives to cholecalciferol and its possible use by the general public 14 Approved (simple majority) Sweden The opinions discussed and adopted at the meeting will be published on ECHA’s website. ECHA also announced that the next meeting will be held on 24–28 November 2025. For questions on this topic or to receive support with your biocidal products, you can contact us. This article was originated from ECHA. Contact with our experts

On 24 July 2025, the European Commission published a Commission Implementing Regulation (EU) in the Official Journal. This regulation amends Regulation (EU) No 564/2013 to adjust ECHA’s fees in line with inflation. According to Article 17 of Commission Implementing Regulation (EU) No 564/2013, fees must be reviewed annually based on inflation. In this context, a cumulative inflation rate of 19.5% was determined by taking into account the average annual inflation rates for the years 2021, 2022, and 2023, and a decision was made to increase the fees accordingly. What does the fee update cover? The amendment solely concerns the adjustment of fees based on inflation and affects the fees related to applications for the placing on the market and use of biocidal products. The new fees will also apply within the European Economic Area starting from 14th August. New Fees Effective from August The updated fees, as determined by the European Commission, are as follows: In Annex I, Table 1 is replaced with the following: Table 1: Standard Fees General description of task; relevant provision in Regulation (EU) No 528/2012 Specific condition or task description Fee (EUR) Approval of an active substance; Article 7(2) Fee for the first product-type for which that active substance is approved 143 400 Additional fee per additional product-type 47 800 Additional fee per product-type (for both the first product-type and any additional product-type) if the active substance is a candidate for substitution in accordance with Article 10 of Regulation (EU) No 528/2012 23 900 Fee for the amendment of an approval, other than the addition of a product-type 23 900 Renewal of an approval; Article 13(3) Fee for the first product-type for which renewal of that active substance is sought 17 925 Additional fee per additional product-type 1 793 Additional fee for the first product-type for which renewal of that active substance is sought in case a full evaluation is found necessary in accordance with Article 14(1) of Regulation (EU) No 528/2012 29 875 Additional fee per additional product-type in case a full evaluation is found necessary in accordance with Article 14(1) of Regulation (EU) No 528/2012 2 988 Additional fee per product-type (for both the first product-type and any additional product-type) if the active substance is a candidate for substitution in accordance with Article 10 of Regulation (EU) No 528/2012 23 900 Inclusion in Annex I of an active substance; Article 28 Fee for the first inclusion in Annex I of an active substance 11 950   Fee for the amendment of an inclusion of an active substance in Annex I   Notification in accordance with Article 17(4) of Commission Delegated Regulation (EU) No 1062/2014 Fee per substance/product-type combination. The fee for the notification shall be deducted from the subsequent application for approval 11 950 In Annex II, Table 1 is replaced with the following: Table 1: Standard Fees General description of task; relevant provision in Regulation (EU) No 528/2012 Specific condition or task description Fee (EUR) Granting of Union authorisation, single product; Article 43(2) Fee per product not identical with (one of) the representative product(s) assessed for the purpose of the substance approval 95 600   Fee per product identical with (one of) the representative product(s) assessed for the purpose of the substance approval 47 800   Additional fee per product when comparative assessment in accordance with Article 23 of Regulation (EU) No 528/2012 is required 47 800   Additional fee per product when the requested authorisation is provisional in accordance with Article 55(2) of Regulation (EU) No 528/2012 11 950 Granting of Union authorisation, biocidal product family; Article 43(2) Fee per family 179 250   Additional fee per family when comparative assessment in accordance with Article 23 of Regulation (EU) No 528/2012 is required 71 700   Additional fee per family when the requested authorisation is provisional in accordance with Article 55(2) of Regulation (EU) No 528/2012 17 925 Notification to the Agency of an additional product within a biocidal product family; Article 17(6) Fee per additional product 2 390 Union authorisation of a same biocidal product; Article 17(7) Fee per product constituting a ‘same product’ within the meaning of Commission Implementing Regulation (EU) No 414/2013  (2) 2 390 Major change of an authorised product or product family; Article 50(2) Fee per application 47 800 Minor change of an authorised product or product family; Article 50(2) Fee per application 17 925 Administrative change of an authorised product or product family; Article 50(2) Fee per notification 2 390 Recommendation on the classification of a change of an authorised product or product family; Article 50(2) Fee per request in accordance with Commission Implementing Regulation (EU) No 354/2013 (3) If the recommendation is to classify the change as an administrative or minor change, the fee for the request shall be deducted from the subsequent application or notification in accordance with Implementing Regulation (EU) No 354/2013 2 390 Renewal of Union authorisation, single product; Article 45(3) Fee per product 5 975   Additional fee per product in case a full evaluation is found necessary in accordance with Article 14(1) of Regulation (EU) No 528/2012 17 925   Additional fee per product when comparative assessment in accordance with Article 23 of Regulation (EU) No 528/2012 is required 47 800 Renewal of Union authorisation, biocidal product family; Article 45(3) Fee per product family 8 963   Additional fee per product family in case a full evaluation is found necessary in accordance with Article 14(1) of Regulation (EU) No 528/2012 26 888   Additional fee per product family when comparative assessment in accordance with Article 23 of Regulation (EU) No 528/2012 is required 71 700 ANNEX II ‘ANNEX III Other fees General description of task; relevant provision in Regulation (EU) No 528/2012 Specific condition or task description Fee (EUR) Technical equivalence; Article 54(3) Fee, when difference between the active substance sources is limited to a change in manufacturing location, and application is based solely on analytical data 5 975 Fee, when difference between the active substance sources goes beyond a

The UK Department for Environment, Food & Rural Affairs (DEFRA) is considering postponing the transitional registration deadlines for chemical substances under UK REACH. A public consultation, launched on 14 July 2025 and open until 8 September 2025, is currently gathering stakeholder feedback on the proposed changes. As is well known, UK REACH (the United Kingdom’s chemical registration system) requires the registration of chemical substances placed on the GB market. However, following the UK’s departure from the European Union, the chemical data sets collected under EU REACH were not transferred to the UK’s Health and Safety Executive (HSE). As a result, many chemical substances on the GB market still require registration under UK REACH. The government continues to work on a new model called the Alternative Transitional Registration model (ATRm). Preliminary drafts of the ATRm were shared with the public during a previous consultation in 2024. However, since the details of the model have not yet been finalized, it remains unclear what data must be submitted and when. According to DEFRA, the government does not anticipate that the data requirements will exceed those proposed in 2024. Given that the legislation needed to implement the ATRm will not be in force in time, it will not be feasible to meet the current registration deadlines of October 2026, October 2028, and October 2030. Therefore, three alternative sets of new deadlines have been proposed for public consultation: Option 1 is the government’s preferred choice as it provides an estimated two-year transition period for finalizing the ATRm and allowing industry time to adapt. Additionally, shortening the gap between registration deadlines from two years to one would still offer adequate time for data collection and submission, while enabling regulators to access information more rapidly and efficiently. The consultation also includes a proposal to extend the deadlines for compliance checks that HSE is required to conduct on 20% of incoming registration dossiers, as stipulated in Article 41(5) of UK REACH. Click here to access DEFRA’s official statement and related documents. For any questions regarding UK REACH, please fill out the form.

On 5 June 2025, the draft Resolution of the Cabinet of Ministers and the accompanying Rules for Joint Submission of Information in Registration Applications under Ukraine REACH were published. These rules were prepared in accordance with Article 38 of the Law of Ukraine “On Ensuring Chemical Safety and Management of Chemical Products” (LCS). According to the announcement published on the MEPR website, the aim of this draft regulation is to establish the procedure for the joint submission of information in registration applications for the same chemical substance under UA REACH. For details, you can visit the announcement page by clicking here. What Does “Draft Rules for Joint Submission of Information” Introduce? Would You Like to Submit Feedback? The Ministry invites feedback from companies, NGOs, academics, experts, and other stakeholders regarding the published draft regulation. All submitted comments will be considered in the preparation of the final version of the text, and revisions may be made accordingly. You can submit your feedback on the draft rules published under UA-REACH to info@mepr.gov.ua by 5 July 2025. Do You Have Questions? For any inquiries on the topic, you may contact info@chemleg.com. Related Services UA REACH Only Representation UA REACH Pre-registration and Registration UA CLP Stewardship

ECHA announced the inclusion of the following substances in the Candidate List on 25 June 2025: Substance name EC number CAS number Reason for inclusion Examples of uses 1,1,1,3,5,5,5-heptamethyl-3-[(trimethylsilyl)oxy]trisiloxane 241-867-7 17928-28-8 Very persistent and very bioaccumulative, vPvB (Article 57e) Used as a laboratory reagent, in cosmetics and personal care products, and in perfumes and fragrances Decamethyltetrasiloxane 205-491-7 141-62-8 Very persistent and very bioaccumulative, vPvB (Article 57e) Used in cosmetics and personal care products, in lubricants and greases, and in automotive care products Tetra(sodium/potassium) 7-[(E)-{2-acetamido-4-[(E)-(4-{[4-chloro-6-({2-[(4-fluoro-6-{[4-(vinylsulfonyl)phenyl]amino}-1,3,5-triazine-2-yl)amino]propyl}amino)-1,3,5-triazine-2-yl]amino}-5-sulfonato-1-naphthyl)diazenyl]-5-methoxyphenyl}diazenyl]-1,3,6-naphthalenetrisulfonate; Reactive Brown 51 466-490-7 – Toxic for reproduction (Article 57c) Used in textile treatment products and dyes *Click here for the source. As with other substances on the Candidate List, these newly added substances are not eligible for the EU Ecolabel award under the EU Ecolabel Regulation. Besides, if they are later included in the Authorisation List, companies will not be allowed to use them unless they apply for authorisation and the European Commission grants permission for continued use. What Does Inclusion in the Candidate List Mean? According to the REACH Regulation, inclusion of a substance on the Candidate List—whether on its own, in mixtures, or in articles—triggers certain legal obligations for companies. For articles containing these substances at concentrations above 0.1%, suppliers must inform consumers about the safe use of their products. ECHA has stated that importers and manufacturers must notify ECHA about any products containing these substances within six months from 25 June 2025. Safety data sheets (SDS) must also be updated accordingly. Chemleg is here to support you in the authorisation and restriction processes under EU REACH. Contact us for assistance. Related Services

On 2 June 2025, the European Commission adopted Regulation (EU) 2025/1090. This regulation introduces new restrictions on the use of N,N-dimethylacetamide (DMAC) (CAS No. 127-19-5, EC No. 204-826-4) and 1-ethylpyrrolidin-2-one (NEP) (CAS No. 2687-91-4, EC No. 220-250-6). With this regulation, Annex XVII (Restriction List) of the EU REACH Regulation has been amended. About the Newly Added Substances N,N-dimethylacetamide (DMAC) DMAC is classified as a Category 1B reproductive toxicant and a Category 4 acute toxicant. The new update introduces the following restriction for DMAC: 1.Shall not be placed on the market as a substance on its own, as a constituent of other substances, or in mixtures in a concentration equal to or greater than 0,3 % after 23 December 2026 unless manufacturers, importers and downstream users have included in the relevant chemical safety reports and safety data sheets, derived no-effect levels (DNELs) relating to exposure of workers of 13 mg/m3 for long-term exposure by inhalation and 1,8 mg/kg bw/day for long-term dermal exposure. 2. Shall not be manufactured, or used, as a substance on its own, as a constituent of other substances, or in mixtures in a concentration equal to or greater than 0,3 % after 23 December 2026 unless manufacturers and downstream users take the appropriate risk management measures and provide the appropriate operational conditions to ensure that exposure of workers is below the DNELs specified in paragraph 1. 3. By way of derogation from paragraphs 1 and 2, the obligations laid down therein shall apply from 23 June 2029 in relation to placing on the market for use, or use, as a solvent in the production of man-made fibres. 1-ethylpyrrolidin-2-one (NEP) 1-ethylpyrrolidin-2-one (NEP) is classified as a Category 1B reproductive toxicant. The following restriction applies to NEP: 1. Shall not be placed on the market as a substance on its own, as a constituent of other substances, or in mixtures in a concentration equal to or greater than 0,3 % after 23 December 2026 unless manufacturers, importers and downstream users have included in the relevant chemical safety reports and safety data sheets, derived no-effect levels (DNELs) relating to exposure of workers of 4,0 mg/m3 for long-term exposure by inhalation and 2,4 mg/kg bw/day for long-term dermal exposure. 2. Shall not be manufactured, or used, as a substance on its own, as a constituent of other substances, or in mixtures in a concentration equal to or greater than 0,3 % after 23 December 2026 unless manufacturers and downstream users take the appropriate risk management measures and provide the appropriate operational conditions to ensure that exposure of workers is below the DNELs specified in paragraph 1. When Will the Regulation (EU) 2025/1090 Enter into Force? Regulation No (EU) 2025/1090 will enter into force on 23 June 2025, and companies are advised to begin preparations accordingly. In this regard, you can find the roadmap we have prepared for companies below. Roadmap for Companies Companies should identify whether DMAC and NEP are used in their products and create an inventory accordingly. For each product or process, it should be checked whether the concentration exceeds 0.3%, and updated SDSs should be requested from upstream manufacturers and importers. Chemical Safety Reports (CSRs) and SDSs should be updated to include the correct DNEL values, and exposure scenarios should be prepared. Necessary personal protective equipment (PPE) should be determined with occupational safety experts. Technical measures such as ventilation, closed systems, gloves, and masks should be implemented in production processes to reduce worker exposure below DNELs. Training documents and work instructions should be revised, and updated SDSs should be shared with customers and distributors. From 23 December 2026, the placing on the market and use of products containing ≥0.3% DMAC or NEP will be prohibited unless DNEL-compliant SDSs, CSRs, and exposure control measures are in place. Companies are strongly advised to be prepared. For companies using DMAC as solvents in the production of man-made fibres, the obligations described above will apply from 2029. For all other sectors, the transition period ends in 2026. Plan Your Compliance Process with Chemleg At Chemleg, we support companies with DNEL calculations, CSR updates, REACH-compliant SDS preparation, and more. You can schedule a meeting with us and start your compliance process immediately. Click here to fill out the form. Related Services

The European Chemicals Agency (ECHA) has redesigned the Classification and Labelling (C&L) Inventory within its chemicals database, ECHA CHEM. The updated inventory is now accessible to users. What is ECHA CHEM? To briefly remind, ECHA CHEM is a platform created by the European Chemicals Agency to improve the use of the largest database in the European Union. Due to the sheer volume of information, users have increasingly found the former database difficult to navigate. To improve usability and accessibility of a database that receives over 30 million views, ECHA developed ECHA CHEM. For more information about ECHA CHEM, you can read this article. What Has Been Updated in ECHA CHEM? To facilitate easier access to classification information for users, the user interface has been improved. Additionally, current and upcoming harmonised classifications at the EU level have been clarified. This aims to support companies in preparing for and implementing necessary safety measures. The C&L Inventory, which includes more than 4,400 harmonised classifications and classifications notified or included in REACH registrations, contains data on approximately 350,000 substances in total. According to ECHA, the updated inventory has been adapted in line with recent legislative changes and designed with future developments in mind. How to Use ECHA CHEM? The video below provides information on how to use ECHA CHEM. For more detailed information about your chemicals, feel free to contact us.  

The Ministry of Environmental Protection and Natural Resources (MEPR) of Ukraine has launched the pre-registration process for chemical substances manufactured and imported at ≥ 1 ton on January 26, 2025. As part of this process, manufacturers, importers, and suppliers are now required to submit information about their chemical substances to the relevant authorities until January 26, 2026. These obligations are being implemented under the Technical Regulation on the Safety of Chemical Products. The aim is to ensure that chemical substances potentially hazardous to human health and the environment are systematically monitored and officially registered. To facilitate a standardized and efficient registration process for all stakeholders, the Ministry has developed a unified pre-registration form, which is now available on the official MEPR website. Companies are instructed to complete this form and send their chemical substance pre-registrations to reach@mepr.gov.ua. For any questions regarding this matter, please feel free to contact us. You can also click here to learn more about our Ukraine REACH registration services.

DEFRA (UK’s Department for Environment, Food & Rural Affairs) has announced updates to certain registration and authorisation fees under UK REACH. The new fees came into effect on 1 April 2025. According to UK authorities, this update is based on the price indices and fee structures proposed by HSE. The updated fee schedule was published on 10 March 2025 under the name The REACH Fees and Charges (Amendment of Commission Regulation (EC) No 340/2008) Regulations 2025. Updated UK REACH Fees Registration Fees Fees for full registrations and intermediate-only registrations have been revised as follows: 1. Standard Fees Tonnage Band Individual Submission Joint Submission All Tonnage Bands £2,222 £2,222 2. Reduced Fees for SMEs Tonnage Band Medium (Ind.) Medium (Joint) Small (Ind.) Small (Joint) Micro (Ind.) Micro (Joint) All Tonnage Bands £740 £740 £399 £399 £57 £57 The lack of tonnage differentiation in standard fees means the base registration cost is the same whether 1 tonne or 1000 tonnes of a substance is manufactured. It is a different approach compared to the EU REACH regulation. However, the reduced fees can help SMEs. A micro-enterprise may pay up to 97% less than a large company for the same registration. Update Fees To maintain transparency and oversight in UK REACH processes, fees for updates under Article 22 have also been revised: Tonnage Band Updates 1. Standard Fees Type of Update Individual Submission Joint Submission All Updates £2,222 £2,222 2. Reduced Fees for SMEs Type of Update Medium (Ind.) Medium (Joint) Small (Ind.) Small (Joint) Micro (Ind.) Micro (Joint) All Updates £1,249 £1,249 £672 £672 £96 £96 Identity Change Identity change fees apply in cases such as mergers, name changes, etc. 1. Standard Fees Type of Change Fee Change in identity of the registrant involving a change in legal personality £290 2. Reduced Fees for SMEs Type of Change Medium Small Micro Change in identity of the registrant involving a change in legal personality £261 £232 £72 Other Changes 1. Standard Fees Type of Update Individual Submission Joint Submission Degree of purity and/or identity of impurities or additives £4,271 £3,203 Relevant tonnage band £1,424 £1,068 A study summary or a robust study summary £4,271 £3,203 Information in the safety data sheet £2,847 £2,135 Trade name of substance £1,424 £1,068 IUPAC name for non-phase-in substances referred to in Article 119(1)(a) of Regulation (EC) No 1907/2006 £1,424 £1,068 IUPAC name for substances referred to in Article 119(1)(a) of Regulation (EC) No 1907/2006 used as intermediates, in scientific research and development or in product and process orientated research and development £1,424 £1,068 2. Reduced Fees for SMEs Type of Update Medium (Ind.) Medium (Joint) Small (Ind.) Small (Joint) Micro (Ind.) Micro (Joint) Degree of purity and/or identity of impurities or additives £2,776 £2,082 £1,495 £1,121 £214 £160 Relevant tonnage band £925 £694 £498 £374 £72 £53 A study summary or a robust study summary £2,776 £2,082 £1,495 £1,121 £214 £160 Information in the safety data sheet £1,851 £1,388 £996 £747 £142 £107 Trade name of the substance £925 £694 £498 £374 £72 £53 IUPAC name for non-phase-in substances referred to in Article 119(1)(a) of Regulation (EC) No 1907/2006 £925 £694 £498 £374 £72 £53 IUPAC name for substances referred to in Article 119(1)(a) of Regulation (EC) No 1907/2006 used as intermediates, in scientific research and development or in product and process orientated research and development (not specified)           PRORD Fees Under Article 9 of the UK REACH Regulation, the fees for PRORD notification and PRORD exemption extension are as follows: PRORD Notification Standard fee £751 Reduced fee for medium enterprise £308 Reduced fee for small enterprise £166 Reduced fee for micro enterprise £24 PRORD notification fees are relatively low compared to other categories, which supports research and development activities. Fees for Extension of PRORD Exemption Standard charge £751 Reduced charge for medium enterprise £617 Reduced charge for small enterprise £332 Reduced charge for micro enterprise £47 Authorisation Application and Review Fees Authorisation Application 1. Standard Fees Application Type Fee Base Fee £57,689 Additional Fee Per Substance £11,538 Additional Fee Per Use £51,920 2. Reduced Fees for SMEs Application Type Medium Small Micro Base Fee £43,267 £25,960 £5,769 Additional Fee Per Substance £8,653 £5,192 £1,154 Additional Fee Per Use £38,940 £23,364 £5,192 Authorisation Review 1. Standard Charges Review Type Fee Base Charge £57,689 Additional Charge Per Substance £11,538 Additional Charge Per Use £51,920 2. Reduced Charges for SMEs Review Type Medium Small Micro Base Charge £43,267 £25,960 £5,769 Additional Charge Per Substance £8,653 £5,192 £1,154 Additional Charge Per Use £38,940 £23,364 £5,192 Authorisation and review fees are notably high, representing a significant cost for companies dealing with SVHCs. Firms are advised to support their applications with thorough justification and explore safer alternatives. Strategic Recommendations • Cost PlanningCompanies are advised to prepare annual budgets that consider costly processes like authorisation and review. • SME DeclarationTo benefit from reduced fees, companies must complete their SME declarations accurately and on time. • Alternatives to SVHCsWhere possible, firms should prioritize substitution of SVHCs to avoid the authorisation process. • Consultancy SupportErrors in these processes may lead to serious financial consequences; expert guidance is strongly recommended. How Chemleg Consultancy Can Help At Chemleg, we support companies in navigating UK REACH registration, notification, and authorisation processes, including: • Development of compliance strategies• Accurate SME declarations• Technical dossier and IUCLID preparation• Data sharing management for lead registrants and obtaining Letter of Access (LoA) for co-registrants with LoA-Pro. Learn more about our UK REACH registration services.