We use cookies to understand site performance and improve follow-up from our team.
For your role
Chemical regulatory work is a moving target. REACH dossiers, SVHC updates, CLP re-classifications, SDS in fifteen languages, poison centre notifications with UFIs, biocides and cosmetics ingredient files feeding back into brand customers. Every customer wants a slightly different SDS in a slightly different format, and every annex update ripples into hundreds of substances. Worldover puts the substance model at the centre, so REACH, CLP, GHS and downstream customer documents all read from one truth, and Willow drafts what your team used to type.
Quick answer
Chemical regulatory affairs software helps a Regulatory Affairs Manager run REACH registration and updates, CLP classification and labelling, GHS-compliant SDS authoring in every required language, poison centre notification with UFI, biocides files and customer-specific documentation. Worldover consolidates all of it on a substance-first data model with Willow drafting from live composition. Typical outcomes: 40 to 60% reduction in SDS authoring time, near-zero missed re-issues after CLP annex updates, and customer documentation packs generated on shipment instead of on request.
How this connects to Worldover
Keeping SDS, REACH and CLP current across a growing substance master?
Worldover holds the substance, mixture, SDS and label as one live record so REACH, CLP and multi-market SDS regenerate the moment the underlying data changes.
See AI ERP for chemicalsBuilt for: Regulatory Affairs Managers at specialty chemical manufacturers, ingredient suppliers and distributors handling 50+ substances across two or more markets, with real SDS authoring load and customer documentation obligations.
Not the right fit for: single-substance producers with no downstream mixture work, or teams that fully outsource SDS authoring to a service and don't want to bring it in-house.
Every substance has one master record: identity, composition, hazard classification, physical-chemical properties, toxicology and ecotoxicology, REACH status, regulatory annex flags. Every mixture inherits from its substances. Every SDS, label and notification reads from that record. Change the classification once, everything downstream updates.
Worldover for this
Pick one substance from your portfolio, ideally one with EU + UK + US exposure. In 20 minutes a Worldover regulatory lead will walk it end to end: REACH position, CLP classification, GHS SDS in three languages, poison centre notification with UFI, and how a hypothetical CLP annex change would ripple into every affected mixture. You leave with a clear picture of the manual work this removes.
Book a chemicals demoWillow drafts GHS-compliant SDS in every required language from the mixture composition and its substances' hazard data. The regulatory manager reviews, questions, approves. Section 15 pulls from the live regulatory map (REACH, TSCA, DSL, IECSC, K-REACH, etc). Customer-specific templates apply without duplicating source data.
Willow monitors ECHA annex updates, SVHC list changes, ATP publications and equivalent feeds. When a substance's classification or status changes, every affected mixture surfaces in the queue with the required action: reclassify, reissue SDS, update label, re-notify poison centre. No manual mapping.
Worldover generates PCN dossiers with UFIs per market, tracks submission status across ECHA and national portals, and re-issues when composition or classification changes. UFIs are managed on the mixture record and printed on the label automatically.
Every shipment can carry the customer-specific pack: SDS in the customer's language and template, TDS, CoA, REACH declaration, RoHS statement, conflict minerals response. Generated on shipment, delivered with the goods, logged for audit.
FAQs
Related
A 20-minute working session. Your SKUs, your customers, your documentation. No slide deck.