HomeProcess
Simple, transparent, documented.
Submit
Send your product details and any existing documentation.
Share your formulation, existing SDS or label, and target market. The more you provide, the faster we can move - but we can also start from a data gap and build the file up with you.
Assess
We evaluate hazards and check for data gaps.
We classify the substance or mixture against CLASS 2013, identify what evidence is missing, and map the route to a complete, defensible classification before any authoring begins.
Author
Documents are drafted, justified and cross-checked.
We draft the SDS, classification record or label in EN and BM, record the justification for every statement, and cross-check the output against the regulations and your own product data.
Deliver & support
Audit-ready files handed over, with revision support.
You receive version-controlled, audit-ready files plus the supporting rationale. As your products or the regulations change, we keep the documents current.
Find your gaps before the regulator does.
Tell us about your product and target market - we will tell you exactly what compliance requires.
Response within 1 business day