Applicable rules
Which laws apply to each product in each market: hazard communication, inventories and registration, notifications and product-specific rules.
A side-by-side view of what applies to your products in Canada, the US, the EU and the UK, where you already comply and what is missing, with a plan to close each gap.
Which laws apply to each product in each market: hazard communication, inventories and registration, notifications and product-specific rules.
Every obligation marked as met, to check or missing, for every market in scope.
The order in which to close the gaps, with the deadlines that drive it and an estimate of the work involved.
Who carries each duty in each market: manufacturer, importer, distributor or, under REACH, an only representative.
Which SDSs and labels can be adapted, and which need to be written from scratch.
A call to go through the findings with your team and answer questions.
The matrix shows where you stand. The roadmap turns it into an ordered list of actions with the dates that drive them.
| Obligation · example | CA | US | EU | UK |
|---|---|---|---|---|
| SDS format and content | Met | Check | Gap | Gap |
| Label content and language | Met | Met | Gap | Check |
| Supplier based in the market | Met | Met | Gap | Gap |
| Substance inventory or registration | Met | Met | Check | Gap |
| Poison centre notification | N/A | N/A | Gap | Check |
| Product-specific rules | Met | Check | Check | Check |
A compliant SDS is only part of market entry. These are some of the obligations a gap assessment checks for.
Products sold to the public fall under the Consumer Chemicals and Containers Regulations, 2001, with their own labels, instead of WHMIS. Health Canada has consulted on changing this.
Manufacturers and importers must notify Health Canada within 10 days after first selling a cosmetic in Canada.
A chemical substance manufactured in or imported into the US must be on the TSCA Inventory or be exempt.
Substances manufactured in or imported into the EU at one tonne or more a year must be registered.
Mixtures classified for health or physical hazards need a poison centre notification and a UFI on the label.
EU registrations and notifications do not cover Great Britain, which has its own UK REACH and GB CLP duties.
You tell us the products and target markets, and we agree what is in scope.
The rules that apply to each product in each market are mapped.
Your current documents and processes are compared against each obligation.
You receive the gap matrix, a prioritised plan and a walk-through call.
WHMIS supplier duties, the Domestic Substances List, consumer chemical and cosmetic rules.
HazCom, the TSCA Inventory, and consumer product rules where products are sold to the public.
REACH registration, CLP, poison centre notification and product-specific regulations.
UK REACH, GB CLP, and EU CLP for Northern Ireland.
Ideally before you commit to a launch date in a new market, because some obligations, such as registration or notification, take time and must be completed before the first sale.
Yes. It covers hazard communication, chemical inventories and registration, notifications, and the product-specific rules that apply to your sector, such as cosmetics or consumer chemical products.
The roadmap estimates the work for each gap, and we can quote fixed fees for any part we would handle.
Yes. Scope it to the market you are entering next. The matrix can be extended later.
Send one SDS for a free spot-check. You get a short written summary within one business day.