REACH review
Confirm substance, role in the supply chain, tonnage context, intended use, destination and the current status relevant to the transaction. A supplier name alone does not establish coverage.
Regulatory & compliance
Documentation that follows the product and the market
Regulatory status is product-, market-, role- and date-specific. We support document review around the actual supply route instead of relying on blanket compliance statements.
Review documentation topicsScope note
Information on this page is a qualification framework, not legal advice or a declaration that every product is registered or compliant in every country. Request the current product-specific status for the intended transaction.
Documentation map
Six reviews before a controlled shipment
Quality and compliance are related, but they answer different questions. Quality governs manufacture, testing and release; compliance connects the supplied material and documents to a market and transaction.
GHS communication
Classification, label elements and SDS content depend on substance or mixture, concentration, jurisdiction and current rules. The destination version should be reviewed before shipment.
Safety Data Sheet
The SDS supports hazard communication, handling, storage, transport and emergency planning. Ask for the current market and language version for the supplied product.
CoA & traceability
A CoA should connect the supplied lot to the agreed specification and release format. The useful level of result detail is established during qualification.
Batch documentation
Specification, manufacturing and testing records, label data, pack identification and shipment references form different parts of the traceability chain.
Export requirements
Dangerous-goods classification, packaging approval, labels, transport papers, customs data and importer responsibilities must be checked for the actual product and route.
Document request brief
Give the document team a route they can verify
A request for “all certificates” is difficult to answer accurately. Four details turn it into a controlled review.
Identify the exact product
Chemical name, CAS, concentration or formulation, grade and intended pack.
Define the market route
Destination country, importer role, use, transport mode and requested language.
List the required evidence
SDS, specification, CoA format, declarations, labels and shipment records.
Confirm current status
Use dated, product-specific documents and record open questions before approval.
Continue the review
Use the page that matches your next decision
Review manufacturing release controls under Quality, request current files in Downloads, or plan destination documents with Global Supply.
Compliance support
Request the current
product document route
Tell us the product, grade, pack, destination, use and the documents your quality team expects.