Pharma Manufacturing

A modern pharmaceutical laboratory transitioning into a digital interface with glowing blue data streams, security shields, and regulatory text representing FDA CSA and EMA Annex 11 compliance.

Computerized System Validation (CSV) in Pharma: 2025 Updates and Preparing for 2026 Compliance

Computerized System Validation (CSV) is no longer a static compliance exercise. In 2025, regulators made that clear. Both the EMA […]

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A women focused on the real-time monitoring and validation of digital systems within a GMP manufacturing environment.

From Setup to Compliance: CSV That Delivers

Case Study / SEQOVA

Discover how SEQOVA supported a pharma manufacturer in achieving full system validation before production go-live. From MES and LIMS to ERP and SCADA, we delivered a structured CSV approach aligned with EU Annex 11—ensuring digital compliance from setup to sustained operations.

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