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GHS Report

GPC Newsletter Aug-2025



Regulatory News

In an effort to combat Canada’s growing opioid crisis, Health Canada under the Government of Canada, has proposed significant regulatory changes to tighten controls over precursor chemicals and designated devices such as pill presses and encapsulators. The proposed changes to the Precursor Control Regulations (PCR) and Schedule IX of the Controlled Drugs and Substances Act (CDSA) were officially published in the Canada Gazette, Part I, on June 28, 2025, and are open for public consultation until August 12, 2025. 

The amendments are designed to disrupt the supply chain for illegally produced fentanyl, which continues to be the primary contributor to overdose deaths nationwide. 

 

What Are Precursor Chemicals and Designated Devices? 

Precursor chemicals are chemical substances that can be used to produce controlled substances such as synthetic opioids such as fentanyl. 

  • Designated devices refer to equipment used in drug production, such as pill presses and encapsulators. The proposed rules would also regulate certain component parts such as  dies,  punches, and  molds. 
  • While these items often are used in legal manufacturing contexts, are increasingly being diverted for illegal drug production in clandestine labs operated by organized crime. 

 

Summary of Proposed Amendments 

According to the documents published in the Canada Gazette, the following regulatory changes are being proposed: 

1. Expanded Import Registration Requirements 

Currently, importers of designated devices (like pill presses) must register their importation with Health Canada. Under the new proposal component parts suitable for use in pill presses and encapsulators such as  dies, molds, punches, would also be subject to registration.  
Importers would be required to provide proof of registration at the time of import. 
 2. New Definitions and Classification 

  • The definition of "designated device" would be updated to include interchangeable or individual components. 
  • Precursor chemicals would be categorized by risk level, allowing more focused regulatory control of high-risk substances (e.g. those commonly linked to fentanyl synthesis). 

 3. Enhanced Compliance and Inspection Powers 

  • Health Canada would be granted broader powers to inspect premises, collect records, and seize non-compliant materials,  including the right to audit production documentation, examine inventory logs, and issue compliance orders. 

 4. Improved Regulatory Flexibility 

The proposed changes would enable faster regulatory response to emerging synthetic drugs, and  
allow provisional controls over new substances or equipment pending formal classification. 
 

Why Are These Changes Necessary? 

Canada is experiencing one of the worst public health crises in its history due to the opioid epidemic. According to national statistics: 

  • Illegally produced fentanyl is involved in over 80 percent of opioid-related deaths in Canada. 
  • Organized crime groups are increasingly using domestic labs to produce fentanyl using imported precursors and unregulated drug manufacturing equipment. 
  • Law enforcement agencies have reported an increase in the illegal importation and diversion of precursor chemicals and components for designated devices. 
     

The regulatory framework aims to: 

  • Prevent the diversion of legally traded materials into illicit drug manufacturing. 
  • Disrupt domestic production capabilities of illegal fentanyl. 
  • Protect communities from the devastating impact of synthetic opioids. 
     

Stakeholder Responsibilities 

If adopted, the new regulations would affect: 

Importers 

  • Must register both designated devices and their components prior to import. 
  • Provide proof of registration to border officers. 
  • Maintain detailed records of sales and storage locations. 
     

Distributors and Manufacturers 

  • Ensure compliance with handling and security protocols. 
  • Participate in inspection procedures by Health Canada. 
  • Report any suspicious orders or diversion risks. 
     

Timeline and Consultation 

  • Publication Date: June 28, 2025 
  • Public Consultation Ends: August 12, 2025 
  • Expected Final Publication: Fall 2025 in Canada Gazette, Part II 
  • Date of Entry into Force: Upon final publication 

 

Access Official Regulatory Texts 

For full details, consult the following Canada Gazette links: 

Conclusion: Strengthening Canada’s Response to the Opioid Crisis 

Canada’s proposed amendments reflect an urgent, evidence-based strategy to combat synthetic opioid trafficking and reduce overdose-related deaths. By extending oversight to chemical precursors and the components of pill-making equipment, the government seeks to disrupt a critical link in the supply chain for illegal fentanyl production. 

Proactive stakeholder involvement during the consultation phase is essential to shaping a balanced regulatory framework that is both enforceable and aligned with legitimate industry needs. 

 

 

In June 2025, the U.S. Environmental Protection Agency (EPA) released its draft risk evaluation for dibutyl phthalate (DBP), also known as 1,2-benzenedicarboxylic acid, 1,2-dibutyl ester (CAS No. 84-74-2) under the Toxic Substances Control Act (TSCA). The draft, and its technical support documents, are now open for a 60-day public comment period and scheduled for peer review by the Science Advisory Committee on Chemicals (SACC) from August 4–8, 2025. 

EPA designated DBP as a High-Priority Substance in December 2019 due to potential risks to human health and the environment. The draft evaluation is part of the agency’s ongoing review process under TSCA to determine whether existing chemicals present an unreasonable risk under current conditions of use (COUs). 

 

Key Findings from the Draft Risk Evaluation   

EPA’s preliminary determination concludes that DBP presents an unreasonable risk of injury to human health from 20 worker-related COUs, 4 consumer COUs, and one environmental COU. These findings are based on exposure scenarios that do not account for the use of personal protective equipment (PPE). However, the report notes that PPE could potentially reduce exposure and mitigate risks. 

Importantly, the agency did not identify unreasonable risks to the general population or from cumulative exposure across conditions of use. Additionally, no unreasonable risk was found for the 19 other COUs considered in the evaluation. 

 

Background and Use of DBP   

DBP is a colorless to pale yellow oily liquid, primarily used as a plasticizer in adhesives, sealants, paints, and coatings. Data from EPA’s 2016 Chemical Data Reporting indicates that U.S. production and import volumes of DBP range from 1 million to 10 million pounds per year. 

EPA's risk evaluation considers various COUs, including: 

  • Use in adhesives and sealants 

  • Paints and coatings 

  • Laboratory chemicals 

  • Commercial and consumer products such as floor coverings, furniture, lubricants, and light sticks 

 

Public Involvement   

Stakeholders can submit comments on the draft risk evaluation through docket EPA-HQ-OPPT-2018-0503 at regulations.gov. EPA encourages active participation from industry, environmental groups, and the public to inform its final risk determinations. 

Further engagement is expected as EPA finalizes the evaluation to ensure transparency and scientific rigor in the chemical safety process under TSCA.

On June 13, 2025, the U.S. Environmental Protection Agency (EPA) issued a final rule in the Federal Register (90 FR 24977), establishing Significant New Use Rules (SNURs) under the Toxic Substances Control Act (TSCA). The rule applies to specific chemical substances that were previously submitted through Premanufacture Notices (PMNs) and are also subject to EPA Orders under TSCA. 

 

Mandatory Notification for New uses 

The rule requires any individual or company intending to manufacture (including import) or process these substances for a “significant new use” to notify EPA at least 90 days in advance. This notification allows EPA to assess potential risks and determine if restrictions are needed before the activity begins. 

 

Effective and Promulgation Dates 

 The rule will take effect on August 12, 2025. For judicial review purposes, the rule will be officially promulgated at 1 p.m. EST on June 27, 2025. 

 

Codification and Compliance 

These SNURs are codified under Title 40 CFR Parts 9 and 721. The affected substances are already subject to risk management provisions in TSCA orders, including exposure control and hazard communication measures. The SNURs ensure that any new or expanded uses beyond these existing terms are properly reviewed by EPA. 

 

Access to Supporting Documents 

Supporting documents and the full rule are available in Docket EPA-HQ-OPPT-2023-0328 on Regulations.gov, and the rule was notified internationally under WTO symbol G/TBT/N/USA/2125/Add.1.

On 2 July 2025, the European Commission released its evaluation of the Waste Electrical and Electronic Equipment (WEEE) Directive, reaffirming its importance in mitigating the environmental and health risks posed by electronic waste. Despite improvements in collection and treatment, the report notes that nearly half of WEEE remains uncollected in the EU, with recycling rates still below target. Identified gaps include limited legislative scope, insufficient recovery of critical raw materials (CRMs), fragmented Extended Producer Responsibility (EPR) implementation, and inconsistent treatment standards. The Commission recommends revising the Directive to address digital and green technologies more effectively, enforce harmonised EPR schemes, and establish mandatory treatment standards to support the EU’s circular economy goals. 

Background  

Electrical and electronic waste is the fastest-growing waste stream in the EU, increasing by approximately 2% each year. In 2022, 14.4 million tonnes of equipment were placed on the market, yet only 5 million tonnes of e-waste were collected. The WEEE Directive addresses this challenge by requiring separate collection and proper treatment, setting targets for recovery and recycling, and applying the polluter-pays principle through EPR. It also seeks to streamline compliance by harmonising national registers and reporting formats across Member States. 

Key Findings 

  • The WEEE Directive remains a relevant and well-aligned policy tool within the EU framework, contributing positively to e-waste management and stakeholder performance. 

  • However, the Directive’s scope is outdated and fails to cover emerging waste streams from CRM-rich technologies such as renewable energy and digital equipment. 

  • Collection rates across the EU remain low, with only a few Member States meeting the 65% target due to economic, infrastructural, and awareness-related barriers. 

  • Recovery of critical raw materials (CRMs), such as copper and rare earth elements is limited as current recycling targets do not sufficiently incentivize their extraction. 

  • Fragmented EPR implementation and inconsistent treatment standards hinder high-quality recycling efforts across the EU. 

Further Step 

As part of the upcoming Circular Economy Act, the European Commission will take the recent evaluation findings into account during the revision of the WEEE Directive, with the aim of enhancing e-waste management and aligning it with broader sustainability goals. 

On 8 July 2025, the European Commission published a wide-ranging legislative proposal package aimed at simplifying the EU’s chemicals legislation. This includes significant proposed amendments to the Classification, Labelling and Packaging (CLP) Regulation, the Cosmetics Regulation, and the Fertilising Products Regulation. The proposals also include a separate regulation that postpones key labelling obligations under the CLP Regulation until 1 January 2028.

 

Key Proposals: Greater Flexibility and Reduced Compliance Burden

The central legislative text (COM(2025) 531) proposes targeted amendments to three major regulations to address compliance challenges, reduce the administrative burden and enhance regulatory clarity across the chemicals sector. Accompanying the proposal is a detailed Annex outlining specific changes to the legal text, which is particularly relevant for compliance teams and legal counsel.

Highlights include:

  • CLP Regulation (EC No 1272/2008):

    • Replaces rigid formatting rules (e.g. fixed font size and black-on-white labels) with readability standards, allowing for greater flexibility across product types.

    • Allows broader use of digital labelling to provide supplementary information online.

    • Revises Article 31 to simplify physical label requirements - label elements must be clear, indelible and contrasting with the background, but a fixed layout is no longer required.

  • Cosmetics Regulation (EC No 1223/2009):

    • Removes the pre-notification requirement for nanomaterials.

    • Introduces clearer procedures for adding new UV filters, preservatives, and colourants to product annexes.

  • Fertilising Products Regulation (EU 2019/1009):

    • Eliminates the need for extended REACH registration for certain component substances.

    • Simplifies the approval process for micro-organisms and introduces digital conformity documentation.

 

Postponement of CLP Amendments to 2028

In parallel, the Commission published a second legislative act (COM(2025) 526) which aims to postpone the implementation of certain controversial provisions introduced by Regulation (EU) 2024/2865. This includes changes to:

  • Label layout and formatting

  • Advertising rules

  • Labelling for online and distance sales

The revised date for the entry into force of these provisions is now set for 1 January 2028, which gives industry more time to adapt.

 

Impact and Next Steps

According to the Commission’s impact assessment, the simplification measures are expected to save the chemicals sector up to €363 million annually without compromising health or environmental protection. These proposals form part of a broader effort under the EU’s Chemicals Industry Action Plan to promote competitiveness and innovation.

The simplification proposal (COM(2025) 531) and the postponement regulation (COM(2025) 526) will now proceed through the ordinary legislative procedure, involving review and potential amendment by the European Parliament and Council.

The UK’s Health and Safety Executive (HSE) has launched an eight-week public consultation on proposed legislative reforms for chemicals regulation in Great Britain. The consultation, which runs until 18 August 2025, invites stakeholders to share their views on planned changes to the GB Biocidal Products Regulation (GB BPR), Classification, Labelling and Packaging (GB CLP), and Prior Informed Consent (GB PIC) regimes.

 

Supporting Economic Growth Through Regulatory Reform

The proposed reforms aim to streamline regulatory processes, reduce costs for businesses, and maintain high standards of health and environmental protection. This initiative is part of the UK Government’s broader Regulatory Action Plan (RAP), which aims to foster innovation and economic growth by modernising regulatory frameworks.

 

Key Proposals Covering Biocides, CLP and PIC

The consultation sets out targeted reforms for three key chemical regulatory regimes:

  • Biocides (GB BPR):

    • Recognising international approvals: The HSE is proposing that biocidal active substances and products approved in trusted foreign jurisdictions to be recognised in Great Britain without the need for a full domestic evaluation. This would significantly reduce the time and cost of bringing products to the GB market while maintaining safety standards.

    • Replacing fixed approval dates with risk-based reviews: Instead of requiring periodic renewals, biocidal active substances and potentially products would remain approved indefinitely, unless ‘called in’ for review based on new evidence of potential risks.

    • Expanding essential use derogations: The reforms would enable temporary authorisations for biocidal products or substances that are essential to society, ensuring the continued availability of critical products while alternatives are sought.

    • Introducing powers for future updates: The HSE is seeking the authority to make technical and procedural changes to the GB BPR through secondary legislation, which would allow for greater flexibility and faster regulatory adjustments.

  • Classification, Labelling and Packaging (GB CLP):

    • Introducing a fast-track classification process: A new, streamlined evaluation route is proposed for substances classified in countries that apply the UN GHS, with transparent processes. This would enable quicker updates to mandatory classifications, reducing regulatory delays.

    • Ending the GB CLP notification requirement: Businesses would no longer be required to notify the HSE when placing new substances on the GB market, easing administrative burdens without compromising safety oversight.

    • Relocating technical notes online: Explanatory notes linked to mandatory classifications would be moved from legislation to the HSE website, allowing for faster updates and simpler access for businesses.

    • Granting powers for general updates: The HSE is proposing new powers to ensure that GB CLP remains aligned with international developments and evolving scientific knowledge.

  • Prior Informed Consent (GB PIC):

    • Removing outdated procedures: The consultation proposes eliminating the Special Reference Identification Number (SRIN) process for small-quantity exports used for research, as this is now considered unnecessary.

    • Simplifying the waiver process: The requirement for explicit consent from importing countries could be streamlined to allow for a more consistent application of waivers for eligible chemicals.

    • Ensuring timely updates: The HSE is also seeking powers to make future amendments to GB PIC more efficiently, thereby ensuring the UK can meet its international obligations without delay.

 

Improving Flexibility

The proposals are designed to give the HSE greater flexibility in decision-making, while ensuring that the UK remains responsive to international scientific developments and avoids unnecessary divergence from global standards. The reforms are also intended to protect the integrity of the UK internal market, including Northern Ireland.

 

How to Participate

Stakeholders, including manufacturers, importers, distributors, NGOs, and members of the public, are invited to submit their views here on the HSE consultation portal by 18 August 2025.

The UK Government has launched a public consultation on proposals to extend the transitional registration submission deadlines under UK REACH further. Published on 14 July 2025 by the Department for Environment, Food & Rural Affairs (Defra), he consultation is open for comments until 8 September 2025.

The current phased deadlines - October 2026, October 2028, and October 2030 - apply to transitional registrations based on the tonnage and hazard profile of the substances. These obligations affect companies placing chemical substances on the market in Great Britain (England, Scotland, and Wales) that were previously registered under EU REACH, but which must now be registered under UK REACH.

Current UK REACH Transitional Registration Deadlines:

Tonnage Band / Substance Type

Current Deadline

≥ 1,000 tonnes/year and

Carcinogenic, mutagenic or reprotoxic substances (CMRs) ≥ 1 tonne/year

Toxic effects to aquatic organisms (acute or chronic) ≥ 100 tonnes/year

Candidate list of substances of very high concern (as of 31 December 2023)

27 October 2026

≥ 100 tonnes/year and

Candidate list of substances of very high concern (substances added between 1 January 2024 and 27 October 2026)

27 October 2028

≥ 1 tonne/year

27 October 2030

 

Not the First Extension

This is not the first time that the transitional registration deadlines have been extended. The original deadlines were set for 27 October 2023, 2025, and 2027. However, following stakeholder concerns about the feasibility of timely compliance, the government consulted on postponement options in early 2023. As a result, the deadlines were formally extended by three years via Statutory Instrument 2023/722, which was adopted in July 2023.

More details on that decision are available here and here.

 

Proposals for Further Delay

As the Alternative Transitional Registration model (ATRm) is still under development, the government is now proposing a second round of deadline extensions. The ATRm is expected to define revised, more proportionate data requirements for transitional registrations. However, the current administration has not yet finalised its implementation, and it is unlikely to be ready in time for the first deadline in 2026.

The consultation presents three options:

Option

Proposed New Deadlines

Comment

Option 1

October 2029, October 2030, October 2031

Government's preferred option: allows two-year transition after ATRm finalisation

Option 2

April 2029, April 2031, April 2033

Longer overall delay, but wider spacing between deadlines

Option 3

April 2029, April 2030, April 2031

Shortest total duration; one-year spacing between phases

 

Compliance Check Timing Also Under Review

The consultation also seeks views on aligning the HSE’s duty to conduct compliance checks (on 20% of dossiers, as per Article 41(5) of UK REACH) with any revised submission deadlines. This ensures that regulatory oversight keeps pace with the updated registration timeline.

 

Consultation Access

Stakeholders are encouraged to submit their feedback before 8 September 2025. The consultation can be accessed here.

On 8 May 2025, the United Kingdom formally notified the World Trade Organization (WTO) of a new regulatory measure titled the Cosmetic Products (Restriction of Chemical Substances) Regulations 2025. This step aims to strengthen consumer protection by revising the permitted levels of benzophenone-3, a common UV-filter used in cosmetic products.

The amendment, which modifies the Cosmetics Regulation (EC No 1223/2009) as it applies in Great Britain, follows expert guidance from the Scientific Advisory Group on Chemical Safety of Non-Food and Non-Medicinal Consumer Products (SAG-CS). The group advises the UK Government independently on chemical risks in consumer goods, with a strong emphasis on safeguarding public health.

Implementation Timeline

Effective Date: 21 January 2026

Transitional Period: Products containing benzophenone-3 already on the market before this date may remain available until 21 July 2026

This move aligns with the UK’s commitment to ensure that only safe cosmetic products are accessible to consumers, reflecting evolving scientific risk assessments and reinforcing public trust in regulatory vigilance.

Türkiye's first comprehensive climate legislation, the Climate Law, has been approved by parliament. This new regulation introduces fundamental changes in greenhouse gas emission reduction and climate change adaptation.

 

Core Objective of the Law

The Climate Law establishes the legal and institutional framework covering greenhouse gas emission reduction and climate change adaptation activities, including related planning and implementation tools, revenues, permits, and oversight.

Emissions Trading System (ETS) - Carbon Credits

One of the most significant innovations of the law is the establishment of an Emissions Trading System (ETS) based on the principle of setting upper limits on greenhouse gas emissions. This system will:

  • Encourage greenhouse gas emission reduction through the buying and selling of allowances

  • Include national and international market-based mechanisms

  • Be organized through primary and secondary markets

 

Carbon Market Board Established

The Carbon Market Board, to be established under the leadership of the Minister of Environment, Urban Planning and Climate Change, will be responsible for the operation of the ETS. The Board will have decision-making authority on critical issues such as the distribution of allowances under the ETS, the amount of allowances to be put up for sale, free allowance decisions, offset ratios, and strategies for the international carbon market.

 

Industry Impact: Incentives and Penalties

The law provides comprehensive incentive mechanisms to support green transformation and climate-friendly investments. Both public and private sectors will be able to benefit from financial support for projects with greenhouse gas reduction and climate change adaptation potential. Revenues from relevant institutions may also be used to promote green capital instruments, develop insurance instruments, and reduce investment risks.

Additionally, according to the new regulation, companies that fail to fulfill their obligations may face significant administrative fines. Penalties vary according to the category of non-compliance and can range from 120,000 TL to 2.5 million TL.

 

Pilot Implementation and Transition Period

A pilot period is envisioned before the ETS implementation begins. During this period, penalties imposed on companies that fail to fulfill their obligations will be applied with an 80% discount. Within three years of the law's entry into force, companies within the ETS scope will be required to obtain greenhouse gas emission permits. When necessary, this period may be extended by up to two years.

 

Implications for the Chemical Sector

The Climate Law represents a watershed moment for Türkiye's chemical industry, which is traditionally energy-intensive and carbon-heavy. Chemical companies will need to:

  • Prepare for mandatory emission monitoring and reporting

  • Develop strategies for carbon allowance management

  • Invest in cleaner technologies to reduce compliance costs

  • Consider carbon pricing in their long-term business planning

The three-year transition period provides crucial time for the chemical sector to adapt to the new regulatory environment while the pilot phase offers an opportunity to test systems with reduced penalties.

The Ministry of Agriculture and Farmers Welfare (Department of Agriculture and Farmers Welfare) has officially notified the inclusion of six new insecticides in the Schedule of the Insecticides Act, 1968 through Notification S.O. 2703(E), dated June 13, 2025. 

The Insecticides Act, 1968 regulates the import, manufacture, sale, transport, distribution, and use of insecticides in India to ensure the safe and effective use of insecticides while minimizing risk to human health, animal welfare, and the environment. The Act also aims to support effective pest control in agriculture and public health through structured regulation and periodic review of permitted substances. 

 

Newly Notified Insecticides 

In exercise of powers under sub-clause (ii) of clause (e) of section 3 of the Insecticides Act, and following consultation with the Central Insecticides Board, the Central Government amended the Schedule to include the following six insecticides: 

Common Name 

CAS Number 

Chemical / IUPAC Name 

Feneptamidoquin 

2132414-06-1 

N-(2R)-[1,3-dimethyl-1-(phenylmethyl)butyl]-8-fluoro-3-quinolinecarboxamide 

Metproxybicyclone 

1848207-89-5 

(1RS,5SR)-3-[2-methoxy-4-(prop-1-yn-1-yl)phenyl]-4-oxobicyclo[3.2.1]oct-2-en-2-yl methyl carbonate 

Tebufloquin 

376645-78-2 

6-tert-butyl-8-fluoro-2,3-dimethyl-4-quinolyl acetate 

Pyrimethanil 

53112-28-0 

4,6-dimethyl-N-phenyl-2-pyrimidinamine 

Tiapyrachlor 

1255091-74-7 

N-[4-chloro-2-(pyridin-3-yl)-1,3-thiazol-5-yl]-N-ethyl-3-(methanesulfonyl)propenamide 

Flumethrin 

69770-45-2 

α-Cyano-4-fluoro-3-phenoxybenzyl 3-[2-chloro-2-(4-chlorophenyl)vinyl]-2,2-dimethylcyclopropanecarboxylate 

These additions reflect the government’s ongoing efforts to strengthen the pest management ecosystem, respond to evolving agricultural challenges, and regulate the use of new chemical compounds entering the market. The inclusion of these substances is expected to enhance farmers’ access to modern crop protection tools while ensuring environmental and public safety. 

 

About the Department of Agriculture and Farmers Welfare  

The Department of Agriculture and Farmers Welfare (DA&FW) is the nodal body responsible for formulating and implementing policies and programs that enhance agricultural productivity and safeguard farmers’ interests. Its mandate includes oversight of crop production, plant protection, agricultural mechanization, crop insurance, and the distribution of essential agricultural inputs. The department works in close coordination with state governments, research institutions, and international organizations to ensure sustainable and farmer-centric agricultural growth throughout India. 

 

Conclusion

The amendment is a significant regulatory update to the Insecticides Act, 1968, which reinforces the government’s commitment to ensuring the safe and effective use of agrochemicals in India. Stakeholders in the agriculture and chemical sectors, including manufacturers, importers, and regulatory bodies, are advised to take note of these additions for compliance and implementation. 

The Ministry of Environment, Forest and Climate Change (MoEF&CC) has issued a Gazette Notification (G.S.R. 438(E)) dated 1st July 2025, introducing a new chapter under the Hazardous and Other Wastes (Management and Transboundary Movement) Rules, 2016. These amendments bring Extended Producer Responsibility (EPR) provisions for non-ferrous metal scrap and will come into effect from 1st April 2026.

Key Highlights

Extended Producer Responsibility (EPR) Framework

The rules cover producers, manufacturers, recyclers, refurbishers, collection agents, and bulk consumers involved in handling scrap or products made from aluminium, copper, zinc, and their alloys.


  • Mandatory Registration: All stakeholders must register on a Centralised Online Portal maintained by the Central Pollution Control Board (CPCB).
  • Recycling Targets: Starting with 10% in 2026–2027, EPR targets will rise to 75% by 2032–2033 (as per Schedule XI).
  • EPR Certificates: Producers can meet targets by recycling themselves or purchasing EPR Certificates from registered recyclers via the CPCB portal.
  • Refurbishment Option: Certified refurbishers can defer EPR obligations temporarily.
  • Audits and Verifications: CPCB or its authorised agencies may audit transactions and compliance regularly.

Mandatory Registration and Digital Compliance

A central online portal will:

  • Manage registrations
  • Track EPR certificates and transactions
  • Monitor compliance through returns and reports
  • Act as a marketplace for EPR certificate trading

Stakeholder Responsibilities

  • Producers & Manufacturers:
    • Ensure collection, recycling, or refurbishing of their products.
    • Meet minimum recycled content use (as per Schedule XIII).
    • Submit half-yearly and annual returns.
  • Recyclers:
    • Recycle scrap in an environmentally sound manner.
    • Maintain transaction records and file returns.
  • Refurbishers:
    • Extend product life through safe refurbishing.
    • Manage and dispose of generated waste responsibly.
  • Collection Agents:
    • Collect and transfer scrap to registered recyclers or refurbishers.
    • File periodic compliance reports.
  • Bulk Consumers:
    • Set up collection points and hand over scrap only to registered entities.

Institutional and Stakeholder Roles

  • CPCB: Administers portal, enforces compliance, issues SOPs, and conducts audits
  • State Governments & SPCBs: Facilitate space for recycling units, conduct inspections, and promote awareness
  • BIS: To update relevant standards within six months
  • Steering Committee: Formed for oversight, dispute resolution, and target review

Penalties & Environmental Compensation

  • Non-compliance may lead to:
    • Revocation of registration
    • Environmental compensation
    • Legal action under Section 15 of the Environment (Protection) Act, 1986
  • Partial refunds of compensation are allowed for late compliance (within 1–3 years)

Important Timelines

Year Recycling Target (% by weight, based on average product life)
2026–2710%
2027–2810%
2028–2930%
2029–3030%
2030–3150%
2031–3250%
2032–33+75%

Milestones

Milestone Deadline
Rules Effective Date1st April 2026
CPCB Portal OperationalWithin 6 months from the rules' commencement
BIS Standards RevisionWithin 6 months
First EPR Target Year2026–2027

Schedules Introduced

  • Schedule X – List of covered non-ferrous metal products
  • Schedule XI – EPR recycling targets timeline
  • Schedule XII – Products allowed for refurbishing
  • Schedule XIII – Minimum recycled content requirements

For More Information: Please visit the Ministry of Environment, Forest and Climate Change or the CPCB website.

On 30 June 2025, China’s Ministry of Industry and Information Technology (MIIT) published the final standard of Desensitized Explosives on the State Administration for Market Regulation (SAMR) portal. MIIT designated new standard GB 30000.30-2025 as Desensitized Explosives. Standard GB 30000.30-2025 refers to the tenth revised edition of the GHS. 

 

Earlier Update in March 2025 

MIIT previously on 4 March 2025 opened the public consultation for the updated version of Desensitized Explosives. Consultation ended on 11 March 2025. More information can be found here

 

Key Insights from the GB 30000.30-2025 

MIIT has included the revised information in the standard of: 

  • Hazard and Precautionary Statements; 

  • Signal word; 

  • Hazard Pictogram; 

  • Classification criteria; 

  • Other provisions 

 

Obligations for Stakeholders 

From 1 July 2026 onwards, all manufacturers and importers of chemicals which classified as desensitized explosives are mandatory to reflect revised information in the labels and safety data sheets (SDS). 

 

Transition Period and Enforcement Dates 

MIIT has started 1 year transition period for stakeholders to adapt to this standard. GB 30000.30-2025 will come into force on 1 July 2026

On July 6, 2025, South Korea proposed a full revision of the “Detailed Handling Standards for Hazardous Chemicals” to align with recent amendments to the Chemical Substances Control Act and the Act on the Registration and Evaluation of Chemicals (K-REACH). These legislative changes shift the management system for toxic substance from a uniform to a differentiated framework based on chemical hazard levels. Consequently, the handling standards for hazardous substances need to be updated to reflect this new approach. 

 

Key Highlights of the Proposed Changes 

A. Updated Objective (Article 1 Draft) 

This regulation aims to establish specific handling guidelines and best practices for hazardous chemicals, as defined under Article 13 of the Chemical Substances Control Act and Rule 8, Annex 1 of its enforcement ordinance. 

B. New Definitions Introduced (Article 2 Draft) 

New terms are defined to clarify the scope of the regulation: 

  • General Standards: Basic safety protocols that all handlers must follow, regardless of the substance’s hazard classification. 

  • Substance-Specific Standards: Detailed handling requirements tailored to each hazardous chemical. 

  • Core Handling Requirements: Mandatory safety measures based on a substance’s known risks. 

  • Recommended Practices: Informational guidelines to support the safe handling of substances on-site. 

C. General Safety Requirements Established (Article 3 Draft) 

All handlers of hazardous substances must adhere to the following protocols: 

  1. Fully understand the safety information before use. 

  1. Wear the appropriate personal protective equipment (PPE). 

  1. Avoid eating, drinking, or smoking near hazardous materials. 

  1. Prevent environmental discharge through proper containment and disposal. 

  1. Inform nearby personnel of potential dangers in case of spills or accidents. 

  1. Dispose of any spilled or leaked chemicals in accordance with legal standards. 

Additionally, employers are responsible for ensuring immediate medical evaluation for workers suspected of exposure to hazardous substances. 

D. New Recommendations by Substance (Annex 1) 

A new annex provides guidance tailored to individual chemicals, supporting safer site-level management. 

E. Updated Hazardous Chemicals List 

The list of regulated substances has been revised and now includes new annotations for clarity and ease of use. 

F. Operational Improvements 

Minor amendments have been made to enhance the regulation’s usability and enforceability. 

 

Public Comments Invited 

Organizations, associations, or individuals who wish to provide feedback on the draft revision must submit their comments to the Chemical Safety Agency by July 27, 2025. Submissions should include relevant contact details and clear feedback on the proposed changes. 

 

On July 8, 2025, South Korea announced the draft establishment of “Standard Quantity Thresholds for Hazardous Chemicals”.  In response to the overhaul of the toxic substance designation and management framework, amendments to the subordinate legislation under the Chemical Substances Control Act are being proposed. The draft introduces specific quantity thresholds for hazardous chemicals, as delegated to the Chemical Safety Agency under Articles 19(2), 19(8), 23(12), 27(1), 27(7), and 29(1) of the enforcement rules. The goal is to establish a clear regulatory basis and update existing thresholds accordingly. 

 

Key Provisions of the Draft Regulation 

A. Classification-Based Quantity Thresholds 

A new reference table is introduced to determine standard control quantities based on the revised classification system under the Act on the Registration and Evaluation of Chemicals. The table covers: 

  • Acute toxicity 

  • Chronic toxicity 

  • Physical and chemical hazards 

  • Ecotoxicity 

Each group is assigned upper and lower threshold limits to reflect hazard severity. 

B. Updated and Expanded Quantity Criteria 

Existing quantity thresholds are revised to align with the updated hazard categories (acute, chronic, and ecological). A new minimum control threshold is introduced for lower-risk substances. 

Additional notes include: 

  • For substances designated as accident-preparedness substances, specific thresholds listed in Annex 3 will apply. 

  • For substances listed as items 282 and 557, if the material is in liquid form under standard conditions, the quantity marked with an asterisk (*) applies. 

  • For entries marked ** or ***, the applicable threshold depends on whether the substance is handled in liquid or solid form. 

C. Consolidation of Existing Standards 

The quantity standards currently found in [Annex 3-2] of the enforcement rules will be migrated and integrated into a separate public notice by the Chemical Safety Agency for clarity and unified management. 

 

Public Comment Submission 

Stakeholders, including institutions, organizations, and individuals, are encouraged to submit feedback on this draft by July 21, 2025. Responses may be submitted online through the National Legislative Participation Center or by sending a written opinion including name, affiliation, contact information, and comments to the Director of the NICS. 

On 14 July 2025, Japan's National Institute of Technology and Evaluation (NITE) published a list of 186 substances classified in accordance with the Globally Harmonized System for Classification and Labelling (GHS) guidelines. NITE released the most recent list for FY 2024 on the portal on behalf of the Ministry of Health, Labour and Welfare (MHLW), the Ministry of Environment (MoE), and the Ministry of Economy, Trade, and Industry (METI), which are in charge of GHS classification in Japan. 

 

Previous update in June 2024 

NITE previously released the FY 2023 GHS list covering 160 substances on its portal on 21 June 2024. More information can be found here.  

 

Important Takeaways from the List  

The FY 2024 list includes 43 newly classified substances and 143 substances with updated GHS classification.  It covers classifications from 1 April 2024 to 31 March 2025.  Furthermore, NITE has supplied comprehensive details including:  

  • CAS and identification numbers;  

  • Classification details;  

  • Hazard class;  

  • Hazard pictogram;  

  • Precautionary and hazard statements;  

  • Reference information and   

  • Signal word 

 

Obligations for Companies  

It is recommended that businesses keep consult the latest GHS data when creating labels or Safety Data Sheets (SDSs).  Nevertheless, using the given classification is not mandatory.  Alternative data or test findings that are not covered by the MHLW, MoE and METI may be used by businesses. 

 

On 18 July 2025, The Ministry of Health, Labour, and Welfare (MHLW) in Japan released a list of substances that have been found to irritate skin or absorb through the skin. The list was made public on the Japan's Workplace Safety Site by MHLW. In addition with this update, MHLW also eliminated three entries from the list.

 

Regulatory Background

The Industrial Safety and Health Regulations, which went into effect on April 1, 2024, stipulate in Article 594-2 that using impermeable protective equipment is required when handling specific substances.  By ensuring that employees are sufficiently shielded from direct exposure to dangerous chemicals, this rule lowers the possibility of skin irritation and other health issues.

 

Obligations for chemical handlers

Employers and employees who handle chemical preparations above the designated cut-off value are required to wear impermeable protective equipment, such as gloves and protective clothes, to shield their skin from potentially harmful compounds.

 

Earlier Update in February 2025

Previously on 26 February 2025, MHLW revised the list of chemicals causing skin irritation. More information can be found here.

 

Key Findings from the Updated Skin Irritating List

Data obtained as of July 14, 2025, is included in 1236 entries of compounds in the updated list. The following details are included in the list:

  • CAS number
  • Name in accordance with the Industrial Safety & Health Act
  • Chemical name in accordance with Japan's GHS classification
  • Additional provisions
  • % Cut-off value
  • Effective date

The Japanese Industrial Standards Committee (JISC) has launched a public consultation on draft standards JIS Z7252 and JIS Z7253, to bring Japan’s chemical communication framework into line with the ninth revised edition of the Globally Harmonized System of Classification and Labelling of Chemicals (GHS Rev. 9) The draft revisions were recently published on the JISC portal. The GHS provides standardized components for communicating hazards, such as labels and Safety Data Sheets (SDS).

 

Regulatory Background

In Japan, GHS-compliant labels and SDSs are required for chemicals governed by the three primary chemical regulations: the Poisonous and Deleterious Substances Control Law (PDSCL), the Industrial Safety and Health Law (ISHL), and the Pollutant Release and Transfer Register (PRTR) Law. The implementation of GHS in Japan is based on the following two key JIS standards:

  • JIS Z7252: Classification of chemicals based on Globally Harmonized System of Classification and Labelling of Chemicals (GHS) and
  • JIS Z7253: Hazard communication of chemicals based on GHS-Labelling and Safety Data Sheet (SDS).

 

Previous update in May 2019

In 2019, Japan adopted GHS Rev. 6 through the mandatory standards JIS Z7252:2019 and JIS Z7253:2019 published on 27 May 2019. More details can be found here.

 

Key Insights from the Draft 

JIS Z7252 (Classification)

  • Explosives: The classification will shift from transport-based (1.1–1.6) to use-based (Divisions 1, 2A, 2B, and 2C).
  • Flammable gases: Category 1B is added (lower flammability); current Category 1 becomes 1A; pyrophoric and chemically unstable gases become subcategories of 1A.
  • Aerosols: Adds "chemicals under pressure" as a new class between high-pressure gases and aerosols.
  • Skin corrosion/irritation: Classification methods for in vitro/ex vivo testing are added to support non-animal testing approaches.

JIS Z7253 (Labelling and SDS)

  • Standard title updated to: "Hazard communication of chemicals based on GHS - Labelling and Safety Data Sheet (SDS)".
  • Annexes A, B, C are  revised to reflect updated hazard/toxicity statements from the UN GHS. New columns added to show revisions.
  • Precautionary statements flexibility expanded; Annex C.4 updated accordingly.
  • Transport information (Annex D.15) is revised to include solids and liquefied gases, in line with the UN GHS update.
  • Annex D updates (D.2, D.4, D.9, etc.) are made to align with revised Industrial Safety and Health Act ordinances and current SDS practices.

 

Comment Period and Enforcement Dates

Stakeholders are invited to submit comments on the draft standards till 9 August 2025. There is currently no official announcement regarding the enforcement date of the standards.

 

 

On 25 July 2025, Japan’s Ministry of Health, Labour and Welfare (MHLW) published draft ordinance for amending the Poisonous and Deleterious Substances List on the country’s e-Gov Public Comment Portal. Fenazaquin has been proposed to get added, whereas formulations containing sodium chlorate or sodium bicarbonate scheduled to get removed from the list. Furthermore, Japan notified the World Trade Organization (WTO) on August 1, 2025, of a draft designating fenazaquin as a deleterious substance.

 

Poisonous and Deleterious Substances List

The Poisonous and Deleterious Substances List under Japan's Poisonous and Deleterious Substances Control Act (PDSCA) classifies chemicals based on their toxicity and health risks, categorizing them as "poisonous" or "deleterious." These substances are regulated for safe handling, storage, and transportation to prevent accidents and ensure public safety. Updated regularly by Japan's MHLW, new substances are added based on scientific evidence. The regulations include safety procedures such as labelling, record-keeping, and reporting to minimize health and environmental risks. Currently there are 587 entries present on the list.

 

Key Insights from the Draft Ordinance

Draft ordinance proposes the following amendments to the list of Deleterious Substances:

  • 4-[2-(4-tert-Butylphenyl)ethoxy]quinazoline (Fenazaquin) (CAS: 120928-09-8) and its preparations (except from those with a concentration ≤19.4%) have been designated as a new deleterious substance.
  • Taking a formulation off the list: Made with sodium bicarbonate (27–37%) (CAS: 144-55-8) and sodium chlorate (47.5–52.5%) (CAS: 7775-09–9), except powdered versions.

It was determined that fenazaquin posed a significant risk of acute toxicity upon exposure, supporting its designation as a deleterious substance. On the other hand, it was found that the sodium chlorate/sodium bicarbonate formulation had far lower toxicity, which justified its removal from the list.

 

Obligations for the Stakeholders

Manufacturers, importers, and distributors of the Poisonous and Deleterious Substances must register their substances with the MHLW and comply with Safety Data Sheets (SDS) and Labelling regulations.

 

Comment Period and Enforcement Dates

Stakeholders are requested to comment on the draft till 24 August 2025. While as per WTO notification, members can comment on the WTO draft till 30 September 2025. Final ordinance will be published in late October 2025. Enforcement is scheduled to be from 1 November 2025 (Except for delisting of entries which will come into effect on the same day of ordinance publication).

On May 13, the Ministry of the Environment and Climate Change (MMA) launched a public consultation on the draft Decree intended to implement Law No. 15.022 of November 13, 2020 on the official page Participa + Brasil. The public consultation, which was open to interested parties on the government’s platform was cancelled a few days later.

The same proposal was then notified to the World Trade Organization (WTO) through a WTO notification. Only WTO Members countries can make comments on the draft, meaning that the general public would not be able to do it. The only plausible way to submit comments from companies and public entities is through national WTO TBT Enquiry Points.

The draft submitted to the WTO remains unchanged from the one published on the page Participa + Brasil. There is no official timeline for the final regulation to be published. Stakeholders are advised to monitor forthcoming developments closely, particularly any updates regarding the implementation timeline and reporting obligations.

Switzerland has officially notified the World Trade Organization (WTO) of a draft revision to the Chemical Risk Reduction Ordinance (ORRChem). The proposal introduces new restrictions on several hazardous substances, aligning with the updated EU REACH regulations and the Stockholm Convention on Persistent Organic Pollutants (POPs). 

The public comment period is open until 27 July 2025, providing stakeholders the opportunity to respond to the proposed measures. 

Objective and Rationale 

The revision aims to strengthen the protection of human health and the environment from harmful chemicals. It also supports international harmonization, the use of safer chemical alternatives, and improved recycling practices, while aligning with EU standards and fulfilling Switzerland's commitments under international treaties. 

Responsible Authorities 

  • The Federal Office for the Environment (FOEN) is the Primary regulatory authority responsible for drafting and implementing chemical safety measures. 

  • The State Secretariat for Economic Affairs (SECO) handles the international trade-related comments and WTO inquiries. 

Key Provisions in the Draft Ordinance 

  1. Ban on Dechloran Plus and UV-328: These substances, as well as mixtures and articles containing them, will be prohibited from manufacture, use, and sale, with limited temporary exemptions. 

  1. PFAS Restrictions: Based on EU Regulation (EU) 2024/2462, PFHxA and its precursors will be banned from various applications, including food contact materials, cosmetics, ski waxes, and paper-based products. 

  1. Microplastic Ban: Preparations containing intentionally added microplastics will be banned, impacting industries such as cosmetics, detergents, fertilizers, pesticides, and artificial sports surfaces. The draft mirrors the phasing and exemptions set out in EU Regulation (EU) 2023/2055. 

  1. Lead in PVC: There will be restrictions on the lead content of PVC products, with exemptions for recycled PVC, which is aligned with EU Regulation (EU) 2023/925. 

  1. Formaldehyde Emissions: Market restrictions on articles and vehicles exceeding formaldehyde emission limits, in line with EU Regulation (EU) 2023/1464. 

  1. Fluorinated Gases and Ozone-Depleting Substances: New controls on hydrofluoroolefins (HFOs), fluorinated ketones, and greenhouse gases in applications such as foams, heating ventilation and air conditioning (HVAC) systems, and aerosols, in accordance with Regulation (EU) 2024/573 and the Montreal Protocol. 

Timeline: 
 
Switzerland notified the draft regulation to the WTO on 28 May 2025. The comment period remains open until 27 July 2025, allowing 60 days for stakeholders to provide feedback. The regulation is expected to be adopted in November 2025, with an intended entry into force on 1 December 2025. 

 

Switzerland has officially notified the World Trade Organization (WTO) of a draft Ordinance on Packaging aimed at reinforcing sustainable packaging practices and advancing the circular economy. The proposed regulation introduces environmental measures that impact the production, design, disposal, and reporting of packaging across all sectors.

The WTO notification was submitted on 10th July 2025, and the public comment period is open until 8th September 2025, allowing stakeholders 60 days to provide feedback on the draft.

Objective and Rationale

The draft ordinance is designed to:

  • Prevent the unsustainable use of resources
  • Promote the circular economy
  • Strengthen environmental protection through improved packaging systems

Responsible Authorities

  • The Federal Office for the Environment (FOEN) is the lead authority responsible for drafting and implementing the proposed regulation.
  • The State Secretariat for Economic Affairs (SECO) is tasked with managing international trade inquiries and WTO-related comments.

Key Provisions in the Draft Ordinance

  • Sustainable Packaging Design: Producers and distributors must, where technically and economically feasible, reduce material use, improve recyclability, and increase the use of secondary raw materials.
  • Extended Take-Back System: A subsidiary take-back obligation will be introduced for non-refillable plastic packaging and beverage cartons, supporting the development of a nationwide separate collection and recycling system.
  • Prepaid Disposal Fees Expansion: The current disposal fee system for glass beverage containers will be extended to cover glass packaging for food and cosmetic products, ensuring the proper financing of waste disposal.
  • Expanded Reporting Requirements: Mandatory reporting obligations will be applied to packaging beyond beverage containers, enabling accurate calculation of recycling rates and fostering transparency in the packaging market.
  • PVC Packaging Regulation Repeal: Existing rules on PVC beverage packaging will be repealed due to its minimal use in the market.
  • Deposit System Simplification: Exceptions to the mandatory deposit scheme on refillable beverage containers will be introduced to streamline usage and encourage reuse.

Timeline

Switzerland submitted the notification to the WTO on 10 July 2025.
The public comment period closes on 8 September 2025.
The regulation is expected to be formally adopted in 2026, with its entry into force scheduled for 1 January 2027.

  • Transition period until 1 January 2028 for take-back obligations
  • Transition period until 1 January 2029 for reporting requirements

On 1 July 2025, the transition period for the introduction of the tenth revised edition of the Globally Harmonized System for Classification and Labelling of Chemicals (GHS 10) was completed.  The South African Department of Employment and Labour previously released Draft Regulation No. 50431, which introduces revised guidelines for limiting exposure to hazardous chemical agents (HCAs).  A key element of the draft is the adoption of GHS 10, which is scheduled to take effect from 1 July 2025.  Comments from stakeholders were due on 5 July 2024. 

Key Updates include: 

  • Adoption of GHS 10 by 1 July 2025, with phase-in schedules for future revisions: 

  • GHS 11: by July 2027 

  • GHS 12: by July 2029 

  • Stricter labelling rules, including pictogram sizes and clearer disclosure of ingredients, especially for carcinogens and Specific Target Organ Toxicity STOT hazards. 

  • Mandatory SDSs for mixtures, even if not classified for acute toxicity. 

  • Revised Occupational Exposure Limits (OELs) with updated calculation methodologies. 

  • Enhanced safety protocols for particulates, confined spaces, and personal protective equipment. 

  • Comprehensive medical and biological monitoring, respecting ethical standards such as informed consent. 

  • Employer obligations to engage health and safety committees in all HCA-related matters. 

For more details, please refer to our previous news update published on GPC gateway

Update: In line with the timeline specified in the WTO notification, Jordan’s standard DJS 990:2024 has entered into force.  Mandatory GHS labelling for chemicals substances and mixtures apply from 1 June 2025. 

 

Original Text: 

On 2 October 2024, the Jordan Standards and Metrology Organization (JSMO) notified the World Trade Organization (WTO) of a draft standard for the labelling of chemical substances. The second edition of the draft standard, DJS 990:2024, is expected to be adopted on 30 December 2024.  

Previously, Jordan had not formally adopted the Globally Harmonized System of Classification and Labelling of Chemicals (GHS). However, this new standard mandates labelling in accordance with the provisions of the 8th revised edition of the UN GHS and the European CLP Regulation (EC 1272/2008). As a Middle Eastern country, this move marks a significant step towards Jordan’s full implementation of the GHS.  

 

Jordanian Technical Regulation 119/2022  

Earlier in 2022, the Jordan Standards and Metrology Organization (JSMO) enacted Technical Regulation 119/2022, which outlines the specific requirements for labelling products that are sold or imported into Jordan.   

  

Scope of DJS 990:2024  

The DJS 990:2024 standard applies to all chemical substances and mixtures, excluding radioactive substances and mixtures, as well as veterinary medicinal products, food or feeding stuffs, cosmetic products, and medical devices.  

  

Insights from the New Labelling Standard  

As per the draft standard, DJS 990:2024, the label should be in both Arabic and English. The main elements that need to be included on the label are as listed below but more information can be found in standard here.  

  • Country of origin and contents  

  • Chemical identifier  

  • Hazard and precautionary statements  

  • Signal word  

  • Hazard class and pictogram  

  

Label and Pictogram Dimensions  

The recommended dimensions for the label and pictogram, depending on the volume of the package are given in the table below.  

Package volume (L)  

Minimum label dimensions (mm)  

Pictogram dimensions (mm)   

Volume ≤ 3   

At least 52 x 74  

At least 10 x 10  

Maximum 16 x 16  

3 < Volume ≤ 50   

At least 74 x 105  

At least 23 x 23  

50 < Volume ≤ 500   

At least 105 x 148  

At least 32 x 32  

Volume > 500   

At least 148 x 210  

At least 46 x 46  

  

Comment Period and Enforcement Date  

The draft is currently open for comment. Stakeholders are invited to comment until 1 December 2024. The standard will come into force on 1 June 2025.   

The Environmental Protection Authority (EPA) of New Zealand has updated its regulatory requirements for businesses that import or manufacture hazardous substances. According to the consolidated Hazardous Substances (Importers and Manufacturers) Notice 2015, with amendments effective from 1 January 2026, all companies handling hazardous chemicals must register key business and product information and submit annual reports on substance quantities. 

 

New Reporting Requirements for Hazardous Substance Importers and Manufacturers in New Zealand 

The revised notice requires all importers and manufacturers of hazardous substances to submit detailed business information to EPA. This includes their 

  • New Zealand Business Number (NZBN) 
  • Registered address and contact person 
  • Company website (if applicable) 

All relevant HSNO approval numbers or group standard titles for each hazardous substance they handle.  

These updates are intended to enhance traceability and improve regulatory oversight of hazardous materials in New Zealand. 

Companies must submit this information within 30 days of first importing or manufacturing a hazardous substance. Any changes, such as a new contact person or updated approvals, must also be reported within 30 days. This system allows EPA to maintain a real-time, accurate register of hazardous substances used or introduced into the New Zealand market. 

 

Annual Reporting of Hazardous Chemicals Now Mandatory 

Beginning with the 2025 calendar year, manufacturers and importers will be required to file annual reports by 31 May each year. These reports must include the total quantities of specified identified substances, including agrichemicals, antifouling agents, timber treatment chemicals, and certain veterinary medicines. The new reporting requirements also applies to explosives manufacturers, who must report the volumes of explosive substances and related components handled during the previous year. 

 

Additional Requirements for Explosives Importers 

Businesses importing explosive materials must comply with even stricter obligations. This includes providing advance shipment information, securing an import certificate, and ensuring materials meet approved standards. These safeguards are intended to reduce the risk of misuse and ensure that national safety and environmental standards are met. 

 

Why These EPA Regulations Matter 

The new EPA rules enhance the oversight of hazardous substances in New Zealand, thereby reinforcing the country’s commitments to environmental protection, chemical safety, and workplace health. By requiring more accurate and timely reporting, EPA will be better equipped to assess environmental risks, improve regulatory enforcement, and develop data-driven policies. 

These updates also position New Zealand alongside other global leaders in chemical regulation and promote safer industrial practices for hazardous materials. Improved data collection also allows for more responsive intervention in case of chemical incidents or non-compliance. 

 

Key Compliance Deadlines and Business Impact 

  • 1 January 2026: The new consolidated EPA Notice takes effect. 
  • 31 May 2026: First annual reports are due, covering activities from 2025. 
  • Ongoing: All first-time importers/manufacturers must register within 30 days. 

 Failure to comply with these updated requirements may result in penalties or enforcement actions under the Hazardous Substances and New Organisms (HSNO) Act. Businesses are urged to review their internal systems and ensure that they can provide EPA with the required records, test data, and accurate quantity reports in a timely manner. 

 

How to Comply with the EPA Importers and Manufacturers Notice 

Businesses can visit the EPA’s official website to access: 

  • The full consolidated notice document 
  • Compliance guidelines and reporting templates 
  • A searchable group standards database for substance classification 
  • Walkthroughs for hazardous substance registration and annual reporting 

This regulatory update underscores EPA’s commitment to improving chemical safety standards across New Zealand. Companies involved in the importation, manufacturing, or distribution of chemicals should begin compliance preparation immediately. 

On 16 July 2025, the United Nations Economic Commission for Europe (UNECE) announced amendments to the Globally Harmonized System of Classification and Labelling of Chemicals (GHS).  The amendments to the tenth revised edition of the GHS were approved by the UN Committee of Experts on the Transport of Dangerous Goods and on the GHS at its twelfth session on 6 December 2024. They will form the basis of the upcoming eleventh revised edition of the GHS. 

The tenth revised edition of the GHS was released on 27 July 2023 on the UNECE portal. More details can be found here

 

Key Updates from the UN Purple Book 2025  

  • Aerosols and Chemicals under Pressure (Chapter 2.3): 
    New provisions provide clearer criteria for the classification of aerosols and chemicals under pressure, ensuring consistency in hazard communication. 

  • Skin Sensitization (Chapter 3.4): 
    Introduces new guidance supporting classification based on non-animal test methods, advancing animal-free toxicology approaches. 

  • Global Warming Hazards (Chapter 4.2): 
    Classification criteria are added for substances and mixtures that are hazardous due to their contribution to global warming, reflecting environmental hazard concerns. 

  • Precautionary Statements: 
    Enhanced rationalization of precautionary statements to improve clarity for users and usability for labelling professionals. 

  • Annex 11 – Simple Asphyxiants: 
    A new section provides guidance for identifying simple asphyxiants to help ensure their proper recognition and risk management. 

The electronic version of GHS Rev. 11 will be available for free on the portal in September 2025

On 16 July 2025, the United Nations Economic Commission for Europe (UNECE) announced amendments to the Model Regulations on the Transport of Dangerous Goods. These amendments to the twenty-third revised edition of the Model Regulations were approved by the UN Committee of Experts on the Transport of Dangerous Goods and on the GHS at its twelfth session on 6 December 2024, and will form the basis of the upcoming 24th revised edition.  

 

Earlier Update in August 2023  

Previously on 10 August 2023, the UNECE released the 23rd revised edition of the Model Regulations on the Transport of Dangerous Goods on its official portal. More details can be found here.   

 

Key Updates from the UN Orange Book 2025 

  • Revised provisions for hybrid batteries containing both lithium-ion and sodium-ion cells, with new entries for batteries in equipment and cargo transport units. 

  • Updated references to the latest ISO standards. 

  • New allowance for the use of recycled plastic materials in flexible intermediate bulk containers (FIBCs). 

  • Clarified packaging requirements for solids that may become liquid during transport. 

  • Introduced provisions for the transport of liquid organic hydrogen carriers (LOHCs). 

  • New rules for salvage pressure receptacles, based on maximum pressure-volume (pV) product. 

  • Added provisions for the classification of energetic samples. 

  • Exemptions for packaging small quantities of environmentally hazardous liquid substances. 

  • Defined requirements for FRP service equipment used in portable tanks, covering design, construction, inspection, and testing. 

The electronic version of 24th revised edition of the Model Regulation will be available for free on the portal in September 2025.  

On 30 July 2025, Ukraine officially notified the World Trade Organization (WTO) of a draft resolution proposing amendments to its Technical Regulation on Cosmetic Products, originally adopted under Cabinet Resolution No. 65 of 20 January 2021. The proposal, submitted by the Ministry of Health of Ukraine, aims to harmonize national cosmetic legislation with Regulation (EC) No 1223/2009 of the European Union — a key step in strengthening product safety, enhancing consumer protection, and reducing trade barriers for cosmetic products.

 

Key Highlights of the Draft Resolution

The draft resolution introduces significant amendments to clauses 38, 39, 47, and 52 of the current Technical Regulation. It also presents updated versions of Annexes 2–6, which include lists of restricted, prohibited, and permitted substances in cosmetic formulations.

1. Alignment with EU Cosmetic Regulation (EC) No 1223/2009

The proposed changes are aimed at ensuring full compliance with updated EU standards, especially those concerning carcinogenic, mutagenic, or reprotoxic (CMR) substances. This alignment is critical for maintaining market access for Ukrainian-made cosmetics in the EU and globally.

2. Ingredient Labelling with INCI Names

To simplify labelling and reflect international practices, the amendments allow the use of INCI (International Nomenclature of Cosmetic Ingredients) names without requiring additional translations into Ukrainian. This streamlines product packaging and enhances cross-border trade efficiency.

3. Revised Labelling Requirements for Packaging

The draft introduces more specific rules for labelling on primary and secondary packaging:

   • If only primary packaging is used, all mandatory labelling elements must be included on it.

   • If secondary packaging is present, the required labelling should appear on the outer (secondary) packaging, while the primary packaging does not need to display the list of ingredients.

4. Transitional Provisions

Provisions have been included for substances listed in Annexes 2, 3, 4, 5, and 6, allowing for a transition period to help manufacturers and importers adjust to the updated requirements.

 

Objectives and Impact

The main objectives of the proposed amendments are:

   • Enhancing consumer information and labelling clarity.

   • Promoting regulatory harmonization with the EU.

   • Facilitating international trade by reducing technical barriers.

By updating its national regulation, Ukraine demonstrates its commitment to aligning with European standards, which is essential for improving market access and protecting consumer health and safety.

 

Legal and Regulatory References

   • The Law of Ukraine “On Technical Regulations and Conformity Assessment”

   • Cabinet Resolution No. 65 “On Approval of the Technical Regulation on Cosmetic Products” dated 20 January 2021

 

Implementation Timeline and Comment Period

The adoption and enforcement dates of the Resolution are yet to be determined. Stakeholders have a 60-day window from the notification date to review and provide feedback on the draft to the Ministry of Economy of Ukraine.

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