Batch management changes
Plan, simulate and execute SAP batch management changes with traceability at every step.
Industries · Pharmaceuticals
SAP batch data for pharma that holds up under a GxP audit
Batch records, material master data and validation environments have to stay traceable under GxP and FDA 21 CFR Part 11.
- Focus
- Batch & material master data
- Compliance
- GxP, FDA 21 CFR Part 11
The problem
A batch management change nobody wants to own
Batch numbering, material master structures and manufacturing execution data have to stay traceable, or a GxP audit becomes a problem. Most pharma companies inherit batch setups nobody fully documented.
Validation and test environments carry the same weight. If test data doesn't reflect real batch and material structures, the validation isn't testing what production will actually run.
Where we help
SAP batch management for pharma
GxP-ready test data
Provision validation systems with production-like batch and material data, masked where needed.
Clean material master data
Deduplicate and standardize material and batch master data before it feeds production.
Cross-system validation
Catch mismatches between quality, manufacturing and SAP data before an audit does.
Benefits
What you get
Traceable batch changes
Every batch management change planned, simulated and logged before it's executed.
GxP-ready test data
Validation environments that reflect real batch and material structures, not stale copies.
Clean material & batch master data
Consistent structures across manufacturing execution and SAP.
Audit-ready data through migration
Batch history and quality records intact when they land in SAP S/4HANA.
Other industries
Where else we work
Our Partners
Next step
Talk to the people who build the tools
Bring your batch management or pharma data problem to the people who build the tools.