Inventories list products, not hazards
A product name tells you nothing. Hazard classification, quantity held and location are what determine your obligations.
The inventory required under the HSW (Hazardous Substances) Regulations 2017, structured so it also does the work you actually need it for — SDS currency, storage segregation, signage triggers and exposure follow-up.
Instant download · Editable .docx + .xlsx
The inventory obligation under the Hazardous Substances Regulations 2017 is one of the few genuinely prescriptive documentation duties in New Zealand work health and safety law, and it is widely met with a spreadsheet listing product names and nothing else. That version fails the moment it is needed — when an SDS has expired, when incompatible substances have been stored together, when quantities have crept over a threshold that triggers signage or additional controls, or when someone needs to know what a worker was exposed to. This register is built to answer those questions.
A product name tells you nothing. Hazard classification, quantity held and location are what determine your obligations.
Safety data sheets have a currency expectation. The register tracks issue date and review date per substance so expiry is visible.
Obligations change with quantity held. A register without a quantity column cannot tell you when you have crossed a line.
This is the inventory and register. Asbestos has its own separate register requirement under different regulations, and location compliance certification is a separate process.
Excel — 6 sheets; Word — 14 pages (procedure + forms) · Formats: XLSX, DOCX
The inventory duty is the anchor, but a register that only satisfies the inventory duty leaves the substantive control obligations undocumented. Both are mapped here.
Written and reviewed by the occupational health and safety team at OH Consultant. Sheet 5 flags substances carrying a workplace exposure standard or biological exposure index, because the inventory is where health monitoring obligations are most often first identified — and most often missed. Quantity thresholds are deliberately left to be confirmed per substance rather than hardcoded, since they vary by classification and change with regulatory amendment.