Composition, hazard classification, safety data, safe handling and regulatory screening.
A chemicals data record should preserve substance identity, composition basis, hazard classification, safety documents, applicable restrictions and the controlled audiences allowed to see sensitive information.
Regulatory content reviewed 8 October 2026
The rules below do different jobs. Some are enforceable sector requirements, some establish the DPP architecture, and some announce future product measures. Each card explains the distinction.
Organize the record in stable blocks so identity, technical facts, evidence and access rules can change without losing provenance.
Defines exactly which model, batch or item the record describes.
Safety data sheets and classification rationale
Connects components, materials, suppliers and facilities.
REACH registrations and supplier declarations
Holds measured, calculated and declared product attributes with their basis.
Laboratory or analytical reports
Maintains repair, use, custody and end-of-life information over time.
Change-controlled formulation records
Safety data sheets and classification rationale · REACH registrations and supplier declarations · Laboratory or analytical reports · Change-controlled formulation records
A battery passport published on DPP Shield: identifiers, materials, substances of concern, carbon footprint, repair information, six evidence documents and a verifiable credential you can check.
Demonstration data for illustration, not a real product.Identify the exact product, economic-operator role, market and applicable legislation.
Map authoritative source records to stable product, operator and facility identifiers.
Review completeness, consistency, access rights and the evidence behind each claim.
Approve a versioned public view while protecting restricted and personal data.
No. It organizes references and product data; it does not replace a legally required safety data sheet or chemical assessment.
Organize at least four governed blocks: Substance or mixture identity and composition basis; Classification, labelling and concentration thresholds; Restrictions, authorisations and substances of concern; Safe-use, storage and disposal information. Every value should retain its source, effective date, product level and review status.
The evidence file should cover Safety data sheets and classification rationale; REACH registrations and supplier declarations; Laboratory or analytical reports; Change-controlled formulation records. A public view can cite approved evidence without exposing restricted files or confidential data.
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