Regulatory partner

Lonza services connect dossiers, SDS, and global chemical compliance

Regulated buyers need more than a material code. They need clear jurisdiction logic, consistent hazard communication, audit-ready document trails, and specialists who understand how fine chemical supply decisions affect registrations, customs, and release planning.

Jurisdiction coverage

Six service tracks for international chemical qualification

Lonza teams help quality, procurement, and regulatory groups assemble consistent evidence packages. Each track is scoped with clear assumptions: substance identity, intended use, annual tonnage, customer geography, and required language formats.

REACH support

Registration status review, SVHC screening, exposure scenario alignment, and tonnage-band documentation for EU supply programs.

TSCA review

Inventory status checks, significant new use considerations, and customer-facing statements for United States manufacturing or import.

KKDIK planning

Turkey registration preparation, representative coordination, and translation-ready substance identity records.

K-REACH checks

Korean substance status, pre-registration evidence, and downstream use clarification for customer qualification files.

China compliance

IECSC screening, new substance flagging, customs data consistency, and SDS localization support.

Japan review

CSCL and ISHL considerations with controlled document responses for pharmaceutical and fine chemical supply chains.

Regulatory matrix with decision-ready outputs

Every regulatory engagement begins with intended market and application boundaries. A pharma intermediate used only under further synthesis may require a different evidence set than a fine chemical sold into a formulated product. Lonza keeps those distinctions visible so compliance language does not drift into unsupported claims.

Region	Primary check	Typical output	Review trigger
EU	REACH EC 1907/2006	Registration or exemption statement	Tonnage, use, SVHC update
US	TSCA inventory	Inventory status memo	New use, import route
Global	GHS SDS	Section 2 hazard communication	Formula, impurity, classification change
Customs	HS alignment	Classification support note	Route, purity, end-use shift

SDS search and document request workflow

Teams can request SDS, CoA, TDS, residual solvent statements, allergen declarations, and change-control contacts through one specialist intake. The workflow captures item number, market, intended use, and language requirement so the first response is useful rather than generic.

Contact regulatory specialist

Start with the market, use, and document gap

Share the target region, molecule family, intended use, and current document need. Lonza will route the inquiry to a regulatory or quality contact who can explain the evidence path and the limits of any statement provided.