HomeProcess

Simple, transparent, documented.

1

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.

2

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.

3

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.

4

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.

06 - Next Step

Find your gaps before the regulator does.

Tell us about your product and target market - we will tell you exactly what compliance requires.

Request free assessment

Response within 1 business day