Data exchanged between WMS and ERP
Product and pack master data, batch, expiry, quality status, location, inventory, receipt, order, pick, pack check and dispatch status require a defined system of record.

Data flow for the Cheb operation
A pharmaceutical WMS is only as reliable as its master data, status logic, interfaces and exception handling. Inter-Pharma defines these requirements for its own warehousing, inventory, picking and dispatch-preparation processes in Cheb. We do not claim to sell proprietary WMS software.
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Product and pack master data, batch, expiry, quality status, location, inventory, receipt, order, pick, pack check and dispatch status require a defined system of record.
Allocation, blocked stock, release status, returns and deviations need documented rules. Actual functionality is verified against the selected system and project scope.
ERP, OMS, PIM, EDI, API or structured files are used only after source, format, frequency, error handling, privacy and approval responsibilities are clear.
Duplicate messages, missing master data, status conflicts, short picks, stock adjustments, interface downtime and temperature or quality holds receive an owner, retry or manual fallback, evidence requirement and escalation time. Access rights and material data changes remain attributable.
Testing covers receipt, quarantine and release, FEFO allocation, expiry and batch blocks, picking, pack verification, dispatch, return, recall traceability, stock reconciliation and controlled recovery after an interface failure. Go-live follows documented acceptance rather than a successful happy-path test alone.
The project covers data and process mapping, roles, test cases, inventory reconciliation, cutover, documented acceptance and controlled start-up. No unverified SLA or software capability is promised.
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