Bulgaria \u00b7 environmental claims and certification \u00b7 law adopted; effective from September 27<\/p>\n
The amendments to the Consumer Protection Act, published on 24 September, introduce new restrictions on environmental claims and sustainability labels from 27 September. A label must be based on a certification system or established by a public authority. Claims about future environmental performance require verifiable commitments, a realistic plan and regular independent verification. Certain general green claims and claims about the climate neutrality of a product based on emission compensation are prohibited. Manufacturers, traders and verification organisations should immediately review labels, advertisements, evidence and the terms of the schemes used. The presence of a management system certificate in itself does not prove every environmental claim.<\/p>\n
Bulgaria \u00b7 e-commerce \u00b7 law adopted; effective from today<\/p>\n
From 24 September, the new Article 52a of the Consumer Protection Act requires a withdrawal function for contracts concluded via an online interface where the consumer has a right of withdrawal. The function must be visible, accessible and available throughout the applicable period, with a clear indication and a separate confirmation. The trader shall send a confirmation on a durable medium with a date and time without undue delay, at the latest by the end of the business day. Online shops and suppliers should check the interfaces, registration records and the process for handling requests. The amendment is important for demonstrating compliance, but does not create a right of withdrawal for every transaction, regardless of the statutory exceptions.<\/p>\n
Bulgaria \u00b7 remote financial services \u00b7 law adopted; effective from today<\/p>\n
With the amendments promulgated on 24 September, the rules for the provision of financial services at a distance are included in the Consumer Protection Act, and the separate existing law is repealed. The new provisions regulate the prior information in Bulgarian, the proof of its implementation and the protection in the case of online conclusion. When using automated means of communication, human intervention is provided at the request of the consumer in the cases specified by the law. Providers should check information packages, archives and interfaces for practices that make informed choice or termination difficult. This is an effective legal change, not a consultation; specific sectoral rules and legal exceptions must be assessed separately.<\/p>\n
Bulgaria \u00b7 digital services and supervision \u00b7 adopted act<\/p>\n
The Instruction No. 3 of July 30, 2026, published on September 24, regulates the interaction between the CRC, the CEM and the CPDP in the supervision under the Digital Services Act. It enters into force upon publication and determines the exchange of information, the coordination of inspections and the work of joint teams. The allocation of competences is essential for providers of intermediary services and platforms, which must maintain traceable responses and evidence. Organizations should verify contacts, internal escalation and the protection of confidential information during inspections. The specified deadlines for exchange between regulators should not be presented as a new universal deadline for response for all providers.<\/p>\n
EU \u00b7 cars and type approval \u00b7 adopted act<\/p>\n
Delegated Regulation (EU) 2026\/1753, published on 24 September, updates the type-approval tables in Annex II to Regulation 2018\/858. The changes link the framework to Euro 7 and relevant UN regulations, including tests for electric vehicles, battery durability and brake emissions. The act enters into force on 25 September, but this does not mean the simultaneous start of all Euro 7 staged requirements. Manufacturers, technical services and approval authorities should check the vehicle category, applicable tests and certificate records. Particular attention should be paid to special vehicles and the grounds for permissible exemptions.<\/p>\n
EU \u00b7 food contact materials \u00b7 correction of non-binding guidelines<\/p>\n
Corrigendum C\/2026\/90069, published on 24 September, corrects a date in the Commission guidance on the application of the restrictions on bisphenol A in food contact materials. On page 11, in the second paragraph, the date 20 July 2029 is replaced by 20 January 2029; the date 20 July 2027 remains unchanged. The correction concerns the clarification of the one-year period for the transfer of ownership of certain reusable final articles. Manufacturers, importers and auditors should correct their work schedules and citations. This is a correction to the guidance and not a stand-alone amendment to the basic Regulation or a new general ban.<\/p>\n
EU \u00b7 aviation and competence \u00b7 amendment of regulation<\/p>\n
Implementing Regulation (EU) 2026\/2111, published and entering into force on 24 September, corrects the dates in Regulation 2025\/2143 on the licensing of air traffic controllers. The aim is to eliminate an inconsistency between the already applicable synthetic training procedures and former military specialists and deferred tasks of the competent authorities. The correction includes the relevant points of Annex II in the earlier implementation regime. Training organisations and aviation authorities should check the authorisation procedures, application files and regulatory versions used. The act does not constitute an automatic recognition of any military licence and does not override the individual assessment of competence.<\/p>\n
EU \u00b7 feed additives and laboratory control \u00b7 adopted act<\/p>\n
Implementing Regulation (EU) 2026\/2110, published on 24 September, authorises essential oil of Origanum majorana as a flavouring feed additive for all animal species under certain conditions. Specifications for composition, analytical control and incorporation through premixtures apply from 14 October. The maximum content is 10 mg\/kg of complete feed with 12% moisture and use in water for drinking is not authorised. Manufacturers and laboratories should check the chromatographic performance, impurities and protection of workers. Separate transitional periods are foreseen for existing additives, premixtures and feed, which should not be confused with the start of the new authorisation.<\/p>\n
EU \u00b7 feed additives and laboratory control \u00b7 adopted act<\/p>\n
Implementing Regulation (EU) 2026\/2113, published on 24 September, authorises Salvia rosmarinus essential oil as a flavouring feed additive under species-specific conditions. The act enters into force on 14 October and sets out the composition, limits for undesirable components and an analytical approach by gas chromatography. Use in drinking water is not authorised. Feed businesses, suppliers and laboratories should verify the species of animals, dosages, identity of the oil and certificates of analysis. The transitional rules foreseen for products already produced apply according to the category and date of production and labelling, and not as a general exemption from controls.<\/p>\n
EU \u00b7 feed additives and laboratory control \u00b7 adopted act<\/p>\n
Implementing Regulation (EU) 2026\/2115 renews the authorisation of menadione sodium bisulphite and menadione nicotinamide bisulphite as feed additives for all animal species. Published on 24 September, the act enters into force on 14 October and repeals Regulation 2015\/2307. Manufacturers should verify the forms of vitamin K3, specifications, analytical methods and up-to-date batch documentation. Appropriate procedures are required to protect users, including against risks from inhalation and skin contact. The transitional rules for existing additives and feed are linked to specific dates of production and labelling and do not replace the verification of the applicable formulation.<\/p>\n
EU \u00b7 sustainability and suppliers \u00b7 delegated regulation adopted<\/p>\n
Today, 24 September, Delegated Regulation (EU) 2026\/1560 on voluntary sustainability reporting enters into force. This is a new legal step under the act published on 21 September, and not a repeat of its adoption. The separate restriction for certain information requests to companies with up to 1,000 employees applies for financial years starting from 1 January 2027. Contracting authorities and suppliers should compare CSRD questionnaires, contractual clauses and evidence with the intended scope. The voluntary standard does not create a general certification obligation for small businesses and does not override information requirements based on other laws.<\/p>\n
France \/ EU \u00b7 wine and geographical indications \u00b7 approved standard amendment to specification<\/p>\n
Communication C\/2026\/4929, published on 24 September, announces the approval of a standard amendment to the specification for the protected geographical indication Atlantique. It covers partially de-alcoholised still red, ros\u00e9 and white wines with an actual alcoholic strength of between 6 and 9 per cent. It provides for mandatory labelling, a declaration of wines intended for de-alcoholisation and systematic checks before and after processing. The amendment concerns producers, control bodies, laboratories and traders using the designation. They must update the analytical and traceability evidence and the labels. This is the announcement of an already approved specification, not an authorisation to use the name outside the defined area.<\/p>\n
France \/ EU \u00b7 foods and geographical indications \u00b7 approved standard specification amendment<\/p>\n
Communication C\/2026\/4964 published on 24 September announces approved changes to the specification for Thym de Provence. Ground dried leaves are added, traceability during grinding is updated and the percentage of stems allowed for the forms indicated is reduced. Storage conditions, deadlines and control points have also been changed. Chromatographic analysis at first harvest from a given plot remains applicable to wild thyme, rather than being presented as a generally abolished control. Producers, processors and auditors should check technological records, batches and labelling against the current specification. The amendment does not extend the geographical area of the protected indication.<\/p>\n
USA \u00b7 pharmaceuticals and market access \u00b7 official guidelines and tariff technical amendments<\/p>\n
On September 23, the US Bureau of Industry and Security published guidance and technical tariff amendments for certain specialty pharmaceutical products. The regime provides for zero additional duty under Section 232 under specific categories and conditions, including origin from eligible jurisdictions, including the EU, or approved urgent health needs. This does not mean exemption from all duties for all drugs. The relevant application path requires product identification, tariff code, origin, and justification. Manufacturers and importers should verify the category, evidence, and applicable time; some of the technical changes begin on September 29. Customs inspection remains independent.<\/p>\n
USA \u00b7 export and technical data \u00b7 current regulatory amendment<\/p>\n
The U.S. Department of State published an effective amendment to the ITAR on September 23, following an erroneous deletion of text in a previous amendment. The provisions of 22 CFR 125.4(b)(10) for certain releases of unclassified technical data by U.S. universities have been restored, as well as portions of the exemptions under 126.1(a). Organizations with U.S. defense technology, international research partnerships, or services should review their current access and transfer procedures. The amendment is not a general liberalization of exports and does not replace the required authorization. Practical solutions require a specific assessment of the technology, the participants, and the applicable exemption.<\/p>\n
Bulgaria \u00b7 inspection and accreditation \u00b7 mandatory transition; reminder T\u20137<\/p>\n
By October 1, 2026, accredited control bodies must submit to the BSA EA a plan for transition to BDS EN ISO\/IEC 17020:2026 and an analysis of the differences compared to the previous edition. The official instructions warn that failure to submit the plan on time will be considered a significant non-conformity under BAS QR 2. This is a reminder seven days before an already announced deadline, not a new change to the standard. Management should check the responsibilities, competence, documents and planned assessments, as well as the proof of sending the package. The plan does not replace the completion of the transition itself: the necessary assessments and corrective actions must be organized according to the separate schedule of the agency.<\/p>\n
EU \u00b7 steel and customs compliance \u00b7 start of implementation; reminder T\u20137<\/p>\n
From 1 October 2026, Implementing Regulation (EU) 2026\/1963 requires evidence of the country of initial melting and pouring of covered steel imports. The main document is the Mill Test Certificate with the country and the number of the melt. During the first year, in the absence of such a certificate, the specified alternative evidence subject to customs control may also be considered. Failure to declare or lack of appropriate verifiable evidence leads to a refusal of the import. Importers must now coordinate the data with manufacturers and suppliers, check the link between documents and batches and prepare the declaration using the relevant TARIC codes. Stand-alone alternatives are only provided until 30 September 2027.<\/p>\n
India \u00b7 electrical products \u00b7 mandatory product conformity; reminder T\u20137<\/p>\n
The Indian Domestic, Commercial and Similar Electrical Appliances Safety Order, SO 1739(E) dated April 6, will come into general application from October 1, 2026. The covered products are required to comply with the specified Indian Standard and BIS Standard Mark under the applicable licensing regime. The scope also includes certain DC or battery powered appliances but excludes products regulated by other orders. Exporters and manufacturers should check the classification, testing and licensing readiness before shipping to India. Later deadlines for certain establishments and special exemptions are not general exemptions. For existing stocks, separate verification of declaration and sale conditions is required.<\/p>\n
India \u00b7 tools and industrial supplies \u00b7 implementation start; reminder T\u20137<\/p>\n
The Indian Hand Tools Quality Control Order, 2025, issued as SO 5596(E) dated 4 December 2025, provides for general implementation from 1 October 2026. The covered hand tools, including the listed pipe wrenches and spanners, shall conform to the specified Indian standards and bear the BIS Standard Mark under license. The table provides for later dates for small and micro enterprises, which shall be verified against the legal status of the manufacturer. European suppliers and their Indian counterparts shall specify the product scope, required testing and permitted marking. This is a reminder of the current schedule and not a new blanket ban on all hand tools.<\/p>\n
India \u00b7 food contact materials \u00b7 product certification; reminder T\u20137<\/p>\n
The general application of Indian Order SO 219(E) for the specified aluminium containers and aluminium beverage cans shall commence from 1st October 2026. The table refers to IS 1660:2024 and IS 14407:2023 and requires BIS Standard Mark under license. For small and micro enterprises, 1st January and 1st April 2027 respectively have been fixed. The scope shall not be extended to all types of kitchenware and packaging. Exporters and importers shall check the specific item, test evidence and stock availability conditions. The Order also contains an exception for items imported already filled with material, which requires verification against the specific shipment.<\/p>\n
EU \u00b7 plant protection and safety \u00b7 start of implementation; reminder T\u20137<\/p>\n
The renewed approval of phosphine under Implementing Regulation (EU) 2026\/1968 applies from 1 October 2026. The conditions for authorisation require trained and authorised personnel, verified gas tightness of the premises and gas supply from the outside. Monitoring of the protective zone with certified measuring devices and appropriate residual gas capture are provided for. For operators, warehouses and testing services, the remaining seven days are an opportunity to check the competence, equipment and records for the safe completion of the processing. This is a renewal of the active substance under specific conditions and not an automatic authorisation for each product. Existing national authorisations and instructions for use must be checked separately.<\/p>\n
EU \u00b7 plant protection and laboratories \u00b7 renewed approval; reminder T\u20137<\/p>\n
The renewed approval of pyraclostrobin under Implementing Regulation (EU) 2026\/1976 starts on 1 October 2026. The act sets out a specification for the active substance and restrictions on significant impurities, as well as attention to the ingredients of the formulations, aquatic organisms and consumer risk from metabolites. Authorisation holders, manufacturers and laboratories should check the specifications used, analytical methods and evidence in the product dossiers. The renewal of the substance does not replace the national authorisation of the specific products and uses. Additional confirmatory information is also required with a separate future deadline. The T-7 reminder is for the start of application, not for a newly published act.<\/p>\n
EU \u00b7 plant protection \u00b7 upcoming renewal; reminder T\u20137<\/p>\n
Implementing Regulation (EU) 2026\/2025 enters into force and applies from 1 October 2026, renewing the approval of mecoprop-P as a candidate for substitution. This status does not imply a general ban, but is essential in the assessment of products and possible alternatives. The conditions focus on the protection of operators, workers, children, birds and non-target plants, as well as residues in food and feed. Authorisation holders and evaluators should review product dossiers, risk mitigation measures and applicable national decisions. The remaining seven days are a preparation period under the already published regime, not a new approval of each formulation.<\/p>\n
EU \u00b7 biocides and industrial processes \u00b7 amendment of authorisation; reminder T\u20137<\/p>\n
On 1 October 2026, Implementing Regulation (EU) 2026\/2024 entered into force, amending the Union authorisation for the LANXESS CMIT\/MIT biocidal product family. The annex with the summary of characteristics has been completely replaced after administrative and minor changes. The regime covers specific products and uses in product types 6, 11, 12 and 13, and not all CMIT\/MIT substances or mixtures. Suppliers and industrial users should check the product identity, authorised use, concentrations and protective measures with the current summary. The review of internal instructions and purchasing documentation should be completed against the applicable conditions, without the change being interpreted as a general prohibition.<\/p>\n
EU \u00b7 disinfection and testing \u00b7 union authorization; reminder T\u20137<\/p>\n
The Union authorisation for ELOCLEAR under Implementing Regulation (EU) 2026\/2028 starts on 1 October 2026. The product uses active chlorine, obtained from sodium chloride by electrolysis, for certain disinfection applications in product types 2 and 4. The authorisation is subject to the specific summary of characteristics and to further demonstration of the accuracy of the analytical method by 1 April 2027. Suppliers and professional users should verify the compliance of the system, the authorised use and the operating conditions. The existence of a Union authorisation does not mean that every electrolysis system or application is automatically covered. The test evidence must remain traceable to the authorised product.<\/p>\n
EU \u00b7 feed, beekeeping and laboratories \u00b7 additive authorisation; reminder T\u20137<\/p>\n
Implementing Regulation (EU) 2026\/2027 enters into force on 1 October 2026 and authorises molybdenum chelate of EDTA as a zootechnical feed additive for honey bees, held by Oligofeed SAS. The authorisation specifies the composition, analytical methods and conditions for inclusion in sugar feed. The use is prohibited in honey stores and during the two months prior to honey collection in order to prevent impurities in honey. Feed manufacturers, laboratories and beekeepers must check the labelling, traceability and protection of workers. This is not a general authorisation for all molybdenum additives or for bumblebees. Practical solutions must follow the authorised formulation and the conditions in the Annex exactly.<\/p>\n
Bulgaria \u00b7 European funding and control \u00b7 institutional rules; reminder T\u20137<\/p>\n
From October 1, 2026, the main amendments to the Organizational Regulations of the Ministry of Finance under Decree No. 133 of September 9 will apply. The act specifies the functions of the National Fund Directorate, including coordination under the NLF and follow-up actions for control, audit and data storage after 2026. Responsibilities under the Social Climate Fund and other financial mechanisms are also specified. Managing structures, implementers and recipients of funds should check the applicable instructions, reporting channels and responsibilities for evidence. This is an institutional change, not a new universal requirement for certification of beneficiaries. Some of the organizational provisions have a separate effective date.<\/p>\n
EU \u00b7 crypto-assets and control systems \u00b7 consultation; reminder T\u20137<\/p>\n
The European Commission is accepting contributions to the targeted consultation on the review of MiCA until 30 September 2026, 23:59 CEST \u2014 1 October, 00:59 in Bulgaria. This is the T\u20137 threshold in Europe\/Sofia time. The procedure is aimed at specialised actors, including crypto-asset issuers, service providers and public authorities. It may inform future assessments and proposals, but does not in itself change existing authorisations or obligations. Affected organisations should prepare concrete examples of difficulties, gaps and evidence of compliance, distinguishing the requested changes from the already applicable rules. The time zone of the form must be respected when submitting.<\/p>\n
EU \u00b7 feed \u00b7 new authorisation; reminder T\u201314<\/p>\n
Reminder two weeks before the start of the regime. Implementing Regulation (EU) 2026\/2061 authorises the combination of narasin and diclazuril Interban for chickens for fattening and chickens reared for laying from 8 October. The authorisation is linked to a specific composition, doses and conditions of use, not to any combination of these substances. Requirements for premixes, incompatibility warnings and a programme for monitoring resistance in Eimeria are included. Feed manufacturers and laboratories must compare formulations, labels, analytical methods and control of cross-contamination. Before delivery, it should be checked that the product, animal species and concentration match the authorisation, including restrictions on co-use.<\/p>\n
EU \u00b7 feed and mineral additives \u00b7 authorization; reminder T\u201314<\/p>\n
Reminder two weeks before the start of the regime. The Implementing Regulation (EU) 2026\/2072 published on 18 September authorises perlite as a technological feed additive for listed categories of poultry and pigs. As of 8 October, the authorisation requires specific purity and control of nickel, respirable crystalline silica and asbestos, in addition to maximum levels in feed. Analytical approaches for identification and composition are foreseen, as well as measures to protect workers. Suppliers and feed businesses should update specifications and acceptance controls, and laboratories should verify methods and necessary limits of determination. The authorisation does not automatically cover all mineral products, all animals or every use of perlite.<\/p>\n
EU \u00b7 feed and microbiological control \u00b7 authorization; reminder T\u201314<\/p>\n
Reminder two weeks before the start of the regime. Implementing Regulation (EU) 2026\/2074 authorises from 8 October a preparation of Bacillus subtilis DSM 33862 and Lentilactobacillus buchneri DSM 12856 as a feed additive. Although intended for all animal species, the authorised use is limited to crushed plant feed materials with a moisture content between 64 and 87 percent. The ratio of strains, the minimum microbial content and the methods for identification and quantitative control are defined. Producers should check the moisture content of the substrate, the traceability of the strains and the storage conditions. It is important for laboratories to distinguish between proof of identity and enumeration of microorganisms and to ensure appropriate verification of the methods.<\/p>\n
EU \u00b7 flavouring additives \u00b7 authorisation and transition; reminder T\u201314<\/p>\n
Reminder two weeks before the start of the regime. Implementing Regulation (EU) 2026\/2076 authorises Myristica fragrans seed oil as a flavouring feed additive under certain conditions from 8 October. The act sets out compositional parameters, including safrole and myristicin, and different permissible levels according to animal category. Conditions are foreseen for inclusion through premixtures, assessment of the combined content with other additives and protection of workers. Transitional periods for existing products are separate from the start of the authorisation. Manufacturers and laboratories should check chromatographic specifications, formulations and labelling. The authorisation should not be transferred to any oils with a similar name or to unintended uses.<\/p>\n
EU \u00b7 poultry and feed \u00b7 amendment of permit; reminder T\u201314<\/p>\n
Reminder two weeks before the start of the regime. Implementing Regulation (EU) 2026\/2077 extends the authorisation of the preparation of benzoic acid, thymol, eugenol and piperine to birds for fattening and birds reared for laying or breeding. The new regime starts on 8 October and replaces Regulation 2015\/1426. Composition limits have also been changed, requiring a comparison of specifications, dosages and analytical evidence. Use with other sources of benzoic acid or benzoates is restricted. Manufacturers should distinguish the newly authorised categories from the old ones for which transitional rules are provided. Laboratory controls should follow the methods for the relevant matrix and not a single common method for all components.<\/p>\n
EU \u00b7 feed and biotechnology \u00b7 authorization; reminder T\u201314<\/p>\n
Reminder two weeks before the start of the regime. Implementing Regulation (EU) 2026\/2079 authorises from 8 October an enzyme preparation of alpha-galactosidase and endo-1,4-beta-xylanase for weaned piglets. The authorisation specifies the production microorganisms, the minimum activities and the methods for their measurement in the additive and feedingstuffs. It is not a general authorisation for all preparations with the same enzyme names. Manufacturers should check the strain identity, the thermal stability during processing and the declared storage conditions. For testing laboratories, the correct use of the GALU and AXC units and the relevant methodologies is essential. When assessing batches, the activity, the matrix and the intended use for the authorised animal category should be confirmed simultaneously.<\/p>\n
EU\/Romania \u00b7 wine and protected origin \u00b7 approved specification; reminder T\u201314<\/p>\n
Reminder two weeks before the start of the regime. Implementing Regulation (EU) 2026\/2106 approves an amendment to the specification of the protected designation of origin Segarcea, which includes the category of quality sparkling wine. The act was published on 18 September and entered into force on 8 October. The approved change covers authorised varieties, technological practices, analytical and organoleptic characteristics, labelling and the link with the geographical area. For producers, traders, laboratories and control bodies, this means a new concrete basis for proving compliance when using the name. Control plans and product files should be updated; the change does not extend protection to wines outside the defined area or outside the approved conditions.<\/p>\n
United Kingdom \u00b7 energy projects and storage \u00b7 consultation; reminder T\u20137<\/p>\n
There is one week left for comments on the formal proposal. Ofgem opened a consultation on the CMP470 amendment to the Connection and Use of System Code on 17 September. It proposes a commitment fee for projects in technologies whose declared capacity significantly exceeds the relevant national targets; the main example discussed is battery storage systems. Comments are being accepted until 5pm UK time on 1 October. For developers and suppliers, this could change the demonstration of project readiness and decisions to join the connection queue. Contracts, security and the realistic nature of timetables will need to be assessed. The document is a preliminary regulatory position and does not yet establish a definitive fee.<\/p>\n
USA \u00b7 pharmacy and manufacturing quality \u00b7 volunteer pilot; reminder T\u20137<\/p>\n
One week left until the next intake, announced on September 21. FDA announces the fifth year of the CDRP pilot program for chemistry, manufacturing, and control readiness in accelerated drug and biologic development. The intake begins October 1, 2026, and is open to up to nine proposals. The program is voluntary and supports discussion of analytical methods, process control, stability, and manufacturing validation; it does not override quality or approval requirements. Developers with applicable U.S. records and their manufacturing partners should review the eligibility criteria and maturity of evidence before planning for an accelerated regulatory pathway.<\/p>\n
Bulgaria \/ EU \u00b7 animal husbandry and veterinary control \u00b7 mandatory veterinary restrictions; reminder T\u201330<\/p>\n
Implementing Decision (EU) 2026\/2052 sets 24 October as the end of the minimum surveillance period for certain areas around outbreaks of sheep and goat pox in the districts of Kardzhali and Yambol. Today, the T-30 threshold is reached by that date. For some of the territories, the protection period continues until 6 October, followed by surveillance from 7 to 24 October. Farmers, transporters and traders should check the exact geographical boundaries and national orders before moving. This is not an automatic authorisation to trade from 25 October: additional restrictions have a separate deadline and the measures may be amended according to the epizootic situation.<\/p>\n
EU \u00b7 steel ropes and market access \u00b7 open formal tender procedure<\/p>\n
The Commission initiated an anti-dumping investigation on 24 September into certain steel ropes and cables originating in India, Thailand and Turkey. The proceedings cover the products specified in the notice with a diameter of more than 3 mm, excluding stainless steel products. This is the initiation of an investigation and not a definitive determination of dumping or imposition of a definitive duty. In order to be included in the sample, certain exporters and unrelated importers must provide information within seven days, by 1 October. European importers and suppliers should immediately verify the product scope, origin and necessary commercial evidence; other procedural steps have separate deadlines.<\/p>\n
EU \u00b7 cellulose ethers and market access \u00b7 open formal tender procedure<\/p>\n
On 24 September, the Commission initiated a separate anti-dumping investigation into certain cellulose ethers originating in China and the Republic of Korea. The scope includes the varieties specified in the notice, used in construction, chemical and other formulations. No definitive anti-dumping duties were imposed by this notice. In order to be included in the sample, certain exporting producers and unrelated importers have seven days, until 1 October, to provide initial information. The companies concerned must verify the chemical identity, tariff code, origin and contractual deliveries. Participation requires traceable data and compliance with separate rules for confidential and non-confidential versions of evidence.<\/p>\n
USA \u00b7 aviation and technical support \u00b7 consultation on proposed directive<\/p>\n
The FAA published a proposal to replace an airworthiness directive affecting certain Textron Cessna 402C and 414A airplanes on September 23. The proposal addresses cracks in engine support elements and provides for updated inspections, replacements, and service life limitations. Comments are being accepted through November 9 under file number FAA\u20132026\u20138818. This is still a proposal, not a definitive new requirement. Operators, maintenance organizations, and suppliers should verify serial numbers, configurations, and available inspection records. For European operations, applicability must be determined separately under the applicable airworthiness regime.<\/p>\n
USA \u00b7 transportation and customs evidence \u00b7 international strategic signal; volunteer pilot<\/p>\n
The U.S. CBP announced on September 23 a voluntary test of an electronic export manifest for road transport in the ACE system. It will begin on October 23, with an expected duration of approximately two years and a limited number of qualified participants. In the pilot, certain initial data is submitted at least 24 hours before departure, and the full manifest is submitted at least two hours before arrival at the final point of departure. This is not a new general mandatory deadline for all carriers. International logistics operators and exporters should evaluate the quality of the data, interfaces and the possibility of participation, as the test may affect future customs processes.<\/p>\n
international \/ Germany \u00b7 accreditation and recognition \u00b7 international strategic signal<\/p>\n
Global ACI announced on September 23 that the German accreditation body DAkkS has joined as a full member. The current official register also confirms its participation in the mutual recognition agreement for the listed activities and sub-levels. The signal is important for laboratories, inspection, certification and verification bodies, as well as for clients relying on cross-border acceptance of results. The specific scope in the register and the accreditation of the relevant body should be checked before use. Historical recognition dates do not imply new approval of all scopes in September; membership does not automatically extend the accreditation of an individual provider.<\/p>\n
EU \u00b7 cybersecurity and supply chains \u00b7 international strategic signal; initial analytical baseline<\/p>\n
The ENISA Threat Landscape 2026 report, published on 22 September, summarises observations on cyber threats in 2025. We include it as an initial strategic guidance, not as a new regulatory act. Vendor dependencies, connected attacks and the dual role of AI as a tool and threat target are particularly relevant for information security audits. Organisations should compare these observations with risk assessments, contractual controls and incident preparedness. The methodology uses publicly available and voluntarily provided data; the results are not a complete count of all incidents and do not demonstrate equal exposure for every organisation.<\/p>\n
EU \u00b7 cybersecurity and oversight \u00b7 operational analytical baseline; audit report<\/p>\n
Special Report 19\/2026 of the European Court of Auditors, published on 21 September and published in the Official Journal on 24 September, assesses the European mechanisms for detecting and responding to cyber incidents. The audit finds partial effectiveness and limitations related to information exchange, reporting and delayed implementation. This is an institutional audit assessment and not a new NIS2 obligation or a new certification scheme. Organisations can use it to check their own escalation procedures, interactions with competent authorities and dependencies on external support. The deadlines set for the European institutions should not be transposed as deadlines for businesses.<\/p>\n
EEA \/ EFTA countries \u00b7 food of animal origin and testing \u00b7 current regulatory baseline; OJ publication<\/p>\n
Decision of the EEA Joint Committee No 157\/2026, published on 24 September, includes Regulation 2025\/2246 on minimum frequencies of official controls for certain residues in food of animal origin. The decision was adopted in June; the September publication is not a new common starting date. We include it as a valid regulatory baseline for cross-border supplies and laboratory work. Competent authorities, businesses and testing laboratories should check the sampling plans, the scope of analyses and the territorial applicability. The explicit derogation for Liechtenstein and the national implementation should be assessed separately, without assuming the same controls for all product categories.<\/p>\n
EEA \/ EFTA countries \u00b7 heavy vehicles and type approval \u00b7 current regulatory baseline; publication in the OJ<\/p>\n
Decision No 163\/2026 of the EEA Joint Committee, published on 24 September, incorporates Regulation 2026\/361 into the framework for heavy-duty vehicles. The act concerns type-approval and on-board monitoring of fuel and energy consumption. This is an initial baseline for the relationship between the EU and EEA EFTA regimes, not a new September date for all technical requirements. Manufacturers, technical services and operators should check the applicable categories, measurement functions and evidence in the approval files. National implementation and transitions under the incorporated Regulation are checked separately for the specific vehicle.<\/p>\n
EEA \/ EFTA countries \u00b7 automated management and testing \u00b7 current regulatory baseline; OJ publication<\/p>\n
Decision No 164\/2026 of the EEA Joint Committee includes Regulation 2026\/481 amending the rules for the type-approval of automated driving systems for fully automated vehicles. The decision was published on 24 September but adopted in June. We note it as a regulatory baseline with implications for testing and cross-border acceptance of approvals. Developers, manufacturers and technical services should check the scope of the system, the test scenarios and the version of Regulation 2022\/1426 used. Inclusion in the EEA alone does not constitute an authorisation for the operation of any automated vehicle and does not replace the specific type-approval.<\/p>\n
EEA \/ EFTA countries \u00b7 food and laboratory control \u00b7 current regulatory baseline; publication in the OJ<\/p>\n
Decision No 166\/2026 of the EEA Joint Committee, published on 24 September, includes a multiannual coordinated programme for the control of pesticide residues for 2026-2028 under Regulation 2025\/854. Specific adaptations are foreseen for the number of samples from Iceland and Norway. The decision was adopted in June and is presented as an active baseline, not as a new programme starting in September. Laboratories, food businesses and competent authorities should match the matrices, substances and analytical capabilities with the programme. The minimum national sampling frequency is not a universal frequency for every business and the exemption for Liechtenstein should be reported separately.<\/p>\n
EEA \/ EFTA countries \u00b7 veterinary medicinal products and GMP \u00b7 current regulatory baseline; publication in the OJ<\/p>\n
Decision No 168\/2026 of the EEA Joint Committee, published on 24 September, includes Regulation 2025\/2091 on good manufacturing practice for veterinary medicinal products. This is the first reflection of the regulatory baseline for the EEA, and not a statement that all manufacturing obligations start on the date of publication of the decision. Manufacturers, importers, contracting authorities and inspection teams should check the quality systems, manufacturing evidence and regulatory references used. In the case of contract manufacturing, it is also important to trace the responsibilities between the participants. The applicable starting dates and transitional conditions under the Regulation itself are assessed separately for the specific activity.<\/p>\n
EEA \/ EFTA countries \u00b7 eco-labelling and product evidence \u00b7 current regulatory baseline; OJ publication<\/p>\n
Decision No 180\/2026, published on 24 September, brings into the EEA updated acts on the EU Ecolabel. They cover criteria for paints, varnishes, specialist coatings and water-based aerosol paints, as well as an extension of criteria for other product groups. The decision was adopted in June and is a strategic baseline for manufacturers, laboratories and bodies assessing applications for the ecolabel. The product group, the wording of the criteria, the evidence of composition and the tests should be checked. An extension of validity for one group does not mean an automatic extension for all certificates or the removal of the check upon renewal.<\/p>\n
EEA \/ EFTA countries \u00b7 aviation organizations and oversight \u00b7 current regulatory baseline; publication in the OJ<\/p>\n
Decision No 178\/2026 of the EEA Joint Committee, published on 24 September, incorporates Regulation 2025\/2293. It amends the requirements for organisations declaring their activities to the competent authority under Regulation 2023\/203 and amends other aviation acts. The alert is an initial regulatory baseline for the EEA and not a new general obligation arising from the September publication date. Aviation organisations and supervisory authorities should verify the legal basis, declarations and evidence in the management systems. The application depends on the exact category of organisation; the declaration regime and separate certification requirements should not be confused.<\/p>\n
EEA \/ EFTA countries \u00b7 maritime transport and emissions verification \u00b7 current regulatory baseline; publication in the OJ<\/p>\n
Decision No 181\/2026 of the EEA Joint Committee, published on 24 September, includes Implementing Decision (EU) 2025\/2452, which updates the list of shipping companies and responsible administration authorities in the emissions trading scheme. The decision was adopted in June and is presented as an operational baseline for administrative traceability. Shipping companies and verifiers should check the identifiers, the competent authority and the route for submitting reports and other evidence. A change to the list does not in itself mean a new methodology for calculating emissions or an exemption from other obligations under the maritime regimes.<\/p>\n
EEA \/ EFTA countries \u00b7 cars and CO\u2082 reporting \u00b7 current regulatory baseline; OJ publication<\/p>\n
Two decisions of the EEA Joint Committee, published on 24 September, update the regulatory references to the CO\u2082 reference emissions for heavy-duty vehicles. Decision No 183\/2026 includes the new values under Regulation 2025\/2335, while Decision No 182\/2026 reflects the corresponding change to the previous framework. This is a common baseline for the input data and the sequence of calculations, not a new universal reduction target that has emerged today. Manufacturers and verification organisations should check the version of the reference values and the assessment models. The publication in September does not replace the independent verification of the dates and transitions in the included acts.<\/p>\n
Published by MG Global in partnership with ERPI.<\/p>","protected":false},"excerpt":{"rendered":"
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