Transform Your Plants into Digitally Intelligent, Patient-Ready Operations.
Legacy MES, siloed data systems, and partially automated environments can’t keep pace with the growing complexity of biologics, personalized medicine, and strict regulatory scrutiny. Producing life-saving therapies today demands more than capacity — it demands connected intelligence.
When manufacturing lacks digitization and orchestration, the fallout is inevitable:
of FDA Form 483 observations relate to process control and documentation lapses
of pharma plants still rely on spreadsheets or paper logs for batch reporting
Pharma, biotech, and CDMO facilities need platforms that go beyond automation — to deliver integrated, compliant, and adaptive production.
Real-time enforcement of recipes, SOPs, and parameter thresholds with automated logging
In-line quality checkpoints, sensor feedback, and trend-based adjustments built into the workflow
Visual OEE tracking, bottleneck heatmaps, and shift-level KPIs with historical comparisons
Replace manual logs with CFR Part 11–compliant digital records and structured review flows
Use sensor, usage, and environment data to trigger maintenance before failure occurs
Workflow-driven tracking of incidents, approvals, root cause analysis, and documentation
Unified data layer connecting materials, lab results, operations, and batch disposition
Cloud dashboards, mobile alerts, and supervisory controls across geographies
In Life Sciences, smart manufacturing is the key to scalability without sacrificing compliance.
We don’t just digitize processes — we engineer compliance-first, data-rich production platforms that connect people, equipment, and decisions.
GAMP 5–aligned design, built-in CFR Part 11 compliance, and validation-ready configurations
Deployable for greenfield or brownfield facilities — scale from one process to full site orchestration
From line-level alerts to enterprise-wide metrics, built for both plant managers and quality leads
Capture signals directly from centrifuges, bioreactors, HVACs, or temperature units and link them to batch context
Harmonize KPIs, material use, and compliance trends across geographies and external partners
Digitize IQ/OQ/PQ workflows, monitor validation drift, and maintain audit-ready logs
INT. makes manufacturing not just smarter — but audit-ready, insight-rich, and globally consistent.
Let’s assess your production stack, identify digital maturity gaps, and define a transformation roadmap that aligns with your operational, quality, and compliance goals.
You’ll receive:
We go beyond maintaining operations—we empower businesses with data, insights, and best practices to stay ahead in an ever-evolving digital landscape.
