01
Supplier GMP claims do not replace batch review
GMP capability is a supplier signal, but each batch still needs COA, assay, contaminant and export document checks.
02
Market requirements differ by destination
US nutraceutical, EU pharmaceutical and Southeast Asia supplement buyers may require different document scope and impurity control.
03
RFQ forms should capture compliance early
Destination market, application, quantity and purity requirement allow the sourcing team to screen documentation before quoting.