Technology when it scales. Expertise when it matters. CHEMREG consultants work alongside your team on interpretation, strategy and defensible decisions — then help you operationalise them.
Registration strategy, dossier support and regulatory representation across REACH, CLP and equivalent global frameworks.
Registration and notification strategy, dossier preparation and updates, substance-evaluation response, only-representative arrangements, and classification and labelling under CLP and equivalent frameworks.
Market-access assessment, obligation mapping and compliance programmes for substances, mixtures and articles.
Obligation mapping across substances, mixtures and articles; market-access assessment for new territories; restricted-substance screening; supply-chain communication and SCIP.
Authoring, review, remediation and multilingual rollout aligned to destination-country requirements.
Authoring and quality review, remediation of legacy documents, extended SDS and exposure scenarios, multilingual rollout, and destination-country format alignment.
Transport classification, documentation and packaging for road, rail, sea and air (ADR, RID, ADN, IMDG, IATA).
Classification for road, rail, inland waterway, sea and air; proper shipping name and packing group determination; documentation, marking, labelling and packaging advice; limited and excepted quantity assessment.
Data-gap analysis, study monitoring, read-across justification and weight-of-evidence assessment.
Data-gap analysis, study design and monitoring, read-across and category justification, DNEL/PNEC derivation, and weight-of-evidence assessment for regulatory endpoints.
Data model design, migration and quality frameworks for compliance-critical substance and product data.
Data model design for substances, compositions and products; migration from spreadsheets and legacy systems; data-quality rules, governance and stewardship operating models.
Inventory notifications, Poison Centre Notification and UFI strategy across EU/EEA and international markets.
Inventory status determination and notification (e.g. TSCA, DSL, K-REACH, KKDIK); Poison Centre Notification dossier preparation; UFI generation and lifecycle management.
Process design, tool selection and rollout to move regulatory work from spreadsheets to structured systems.
Current-state assessment, target operating model, tool selection, phased rollout and change management to move regulatory work into structured, auditable systems.
Products, substances and business processes.
Regulatory obligations and compliance risks.
Processes, data models and digital solutions.
Regulatory content, software and workflows.
Changes, deadlines and continuing obligations.
Whether you need regulatory expertise, chemical data management or intelligent compliance software, CHEMREG can help.