Pharmaceuticals & Life Sciences

Where compliance
meets performance.

Pharmaceutical and life sciences companies operate in one of the most demanding regulatory environments in the world. Every SAP configuration, every integration, every data process must meet GxP, FDA and EMA requirements - without sacrificing operational efficiency.

Zurich DS was built for this environment. Our consultants understand batch release, quality management, GMP manufacturing and the documentation requirements of regulated systems.

We bring both SAP expertise and life sciences regulatory knowledge - so you never have to choose between compliance and capability.

Solutions for pharma

Industry-specific capabilities

Batch Release

SAP QM-based batch release cockpits, usage decisions and electronic batch records aligned to GMP.

GxP Compliance

Audit trails, electronic signatures and change control in SAP meeting 21 CFR Part 11 and Annex 11.

CSV / Computer Validation

GAMP 5-aligned validation of SAP systems and integrations with full lifecycle documentation.

Serialization & Track-Trace

SAP serialization configuration for EU FMD, DSCSA and other national traceability requirements.

LIMS Integration

Validated connections between laboratory systems and SAP QM for result transfer and batch decisions.

Deviation & CAPA

SAP QM workflows for deviation management, root cause analysis and CAPA tracking.

Let's discuss your pharma SAP challenges.

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