# GMP document management systems

LIMS / MES & lab informatics — Dedicated repository platforms that version, route for approval and store controlled GMP documents — SOPs, batch records, validation protocols — as their own linked content layer, distinct from the deviation/CAPA/training hub that a broader eQMS runs on top of those same documents.

Source: https://en.bioecon.ru/market/lims-mes/gmp-document-management-systems/

