Close
Life Sciences
Modernization without complexity
Real-time visibility, digital batch records, and automated quality checks reduce risk, improve release times, and support continuous improvement.
Digitize, standardize, and control every step of your regulated operation
Life sciences manufacturing requires absolute precision, traceability, and process adherence – from the intake of raw materials through formulation, batch processing, filling, and packaging. TilliT provides a fully digital, no-code execution and quality platform that helps pharmaceutical, biotech, medical device, nutraceutical, and other regulated producers operate more safely, more efficiently, and in full compliance with 21 CFR Part 11.
Built for regulated environments
TilliT brings order-centric execution, digital batch records, equipment connectivity, and quality management together in one unified system. Every activity, measurement, deviation, signature, and event is captured automatically, providing complete confidence in data integrity and audit readiness.
- Fully digital batch and device history records
- Electronic signatures with full audit trails
- Configurable workflows for GMP, SOPs, and quality gates
- Complete traceability of materials, equipment, operators, and process parameters
Digital workflow for batch and lot-based processes
Whether running cleanroom operations, sterile fill-finish, or pilot plant experimentation, TilliT orchestrates activities with real-time precision.
- Enforce pre-start checks, line clearance, sanitation, and environmental controls
- Trigger sampling, in-process checks, and QC tasks based on time or production count
- Guide operators through validated process steps with multimedia SOPs
- Automatically correlate equipment events with batch deviations or alarms
Real-time quality and compliance control
Life sciences teams gain full visibility across operations – including in-spec, out-of-spec, pending tests, escalations, and deviations – all in one place.
- Model highly complex material- or customer-specific checks
- Capture QC data directly or from instruments, LIMS, and sensors
- Enforces corrective actions, retests, and holds
- Generate instant audit-ready reports for FDA, EMA, TGA, and other regulators
Machine connectivity and environmental monitoring
Using TilliT Edge, connect directly to equipment, sensors, and PLCs to capture the process variables that matter most:
- Temperature, pressure, flow, speed
- Environmental data (humidity, room conditions, HEPA status)
- Equipment readiness, alarms, cycle states
This ensures stronger deviation analysis, better batch release confidence, and reduced manual transcription.
Accelerate validation and reduce human error
With standardized digital procedures, contextual operator guidance, and AI-assisted recommendations, life sciences manufacturers achieve:
- Faster onboarding and training
- Reduced risk of batch failures and rework
- Higher adherence to validated processes
- Seamless compliance during audits and regulatory inspections
If you manufacture in a regulated environment and need full traceability with operational control, TilliT is purpose-built to support you.
Insights
Want to know more about TilliT MES?
Explore further by scheduling a demo through the form or by reaching out to one of our experts directly. We're here to assist you!
Contact Rafael Amaral
Contact James Balzary
