CHEMREG combines regulatory expertise, chemical science and intelligent digital solutions to help companies manage product compliance across global markets.
Chemical Regulatory Expertise Across the Product Lifecycle
CHEMREG supports chemical manufacturers, formulators, distributors and downstream users with regulatory consulting, product stewardship and digital compliance solutions.
Model a substance or mixture once. SDSFORGE derives classification from your data, applies managed regulatory phrases, and generates SDS documents per destination country and language from one structured source.
Upload inbound supplier Safety Data Sheets and get structured, reviewable regulatory data — identifiers, composition, classification, properties and transport — with provenance and validation at every step.
Work through transport classification from hazard characterisation to UN number, packing group and mode-specific provisions — with the reasoning and inputs attached to every result.
Effective: 01 Jan 2027Impact: MediumLogistics · Manufacturing · Chemicals
Action required
Recommended action — Review affected product classifications and update SDS and label documentation before the application date. Open Regulatory Intelligence →
Why CHEMREG
Where Chemistry, Regulation and Technology Meet
Chemical Expertise
Deep understanding of chemistry, substances, mixtures and material properties.
Regulatory Knowledge
Global product compliance expertise across key chemical regulations.
Digital Technology
Software, automation and AI-supported regulatory workflows.
Practical Compliance
Solutions designed for real operational compliance processes.
Industries
Regulatory Expertise Across Complex Industries
From substance manufacturers to downstream users, CHEMREG supports compliance where the regulatory stakes are highest.
Chemicals
Specialty Chemicals
Pharmaceuticals
Cosmetics
Automotive
Manufacturing
Food & Packaging
Energy
Logistics
Consumer Products
How We Work
From understanding your products to monitoring what changes
1
Understand
Products, substances and business processes.
2
Assess
Regulatory obligations and compliance risks.
3
Design
Processes, data models and digital solutions.
4
Implement
Regulatory content, software and workflows.
5
Monitor
Changes, deadlines and continuing obligations.
Regulatory Intelligence
Know what changed. Know what to do next.
Structured regulatory updates — jurisdiction, regulation, dates, impact and affected products — not a generic news feed.
Canada opens a mandatory CEPA section 71 data call on ~200 substances
Environment and Climate Change Canada and Health Canada published two section 71 notices under CEPA 1999 in the Canada Gazette on 29 August 2026, together covering about 200 substances. Response is mandatory for anyone who manufactured, imported or used a listed substance above the reporting threshold in 2025. Phase 1 (184 substances) closes 3 March 2027; Phase 2 (16 substances) opens the next day and closes 8 September 2027. This is an information-gathering action, not a WHMIS reclassification or a restriction.
Published10 Sept 2026EffectiveNotices in force 29 August 2026Compliance deadlinePhase 1 (184 substances) closes 3 March 2027; Phase 2 (16 substances) runs 4 March – 8 September 2027
European UnionCLP — Regulation (EU) 2024/2865, amended by (EU) 2025/2439IN FORCE
EU CLP transition: formulation changes can end your grace period
Regulation (EU) 2024/2865 changed the CLP framework and, together with Delegated Regulation (EU) 2023/707, brought in new hazard classes (ED, PBT/vPvB, PMT/vPvM). Regulation (EU) 2025/2439 ("stop the clock") then postponed the label-format and advertising provisions to 1 January 2028. The classification duties for the new hazard classes were not postponed: substances already on the market are due on 1 November 2026, mixtures already on the market on 1 May 2028. The transition rules are not only about dates — placing a reformulated mixture on the market can end the grace period the original mixture relied on.
Published10 Sept 2026Effective2024/2865 in force 10 December 2024; 2025/2439 ("stop the clock") in force 23 December 2025Compliance deadlineNew hazard classes for substances already on the market: 1 November 2026. Label-format and advertising rules: postponed to 1 January 2028. A reformulation can remove a mixture's transitional protection.
United StatesTSCA Section 5 (New Chemicals Program)UPDATED
EPA New Chemicals data shows submitter-side delays hold up market entry
EPA's New Chemicals Program status pages show a familiar pattern: cases sitting in risk assessment, and cases waiting on the submitter to sign a consent order. The useful takeaway for companies is that regulatory delay is not always EPA's doing. Incomplete information, unresolved exposure data and slow internal order-signature workflows can add weeks or months to a launch. New-chemical approval is best run as a launch-readiness discipline, not a filing you hand off and wait on.
Published10 Sept 2026EffectiveObservation from EPA New Chemicals Program status pages, September 2026. No fixed date — review time depends on submission completeness and internal order-signature turnaround.
