CIPA turns
shop-floor data
into lasting performance
An integrated platform to orchestrate quality, production, maintenance and R&D in regulated environments, and accelerate continuous improvement with AI.
- Unified data
- Controlled processes
- Stronger compliance
From bulk active ingredients to final blister packaging, CIPA helps pharmaceutical labs secure regulatory compliance, optimize eBR and speed up batch release.
4 ways CIPA strengthens core pharmaceutical operations
Browse the cards to explore each lever: the data, the visuals and the before/after CIPA comparisons.
Strengthen FDA & GMP regulatory compliance
Comply with strict FDA (21 CFR Part 11) and GMP guidelines through automated audit trails and complete digital traceability of every step.
- Slow, risky manual audit preparation
- High risk of paper transcription errors
- Compliance data fragmented in silos
- Audit trail hard to rebuild by hand
- 100% automated audit trails
- Strict compliance with 21 CFR Part 11
- Dual approval and electronic signatures
- Instant compliance reports and audits
Formula file approval
GMP specifications approved
Operator & pharmacist dual signature
Electronic signature record active
FDA audit-trail archiving
Report generated & signed per 21 CFR Part 11
3 ways CIPA accelerates product safety, innovation and sustainable performance
Three growth levers, illustrated with concrete data and results measured at our customers’ sites.
Accelerate innovation and optimize R&D transfer
Ease technology transfer between R&D labs and the production plant. Centralize formulas and standardize recipes to speed up drug industrialization.
- R&D-to-plant formulation transfer on paper
- Complex, undocumented scale-up
- Long, costly new drug launches
- Errors when adapting formulas for production
- Single repository of standardized digital formulas
- Seamless collaboration between labs and plants
- Documented, automated scale-up
- Dramatically shorter time-to-market
One platform for excellence, traceability and 21 CFR Part 11 compliance.
CIPA unifies people, processes and data to deliver connected insights across the pharmaceutical value chain — patient safety, ALCOA+ data integrity, automated compliance audits and real-time eBR.
How CIPA works
Five steps, one measurable continuous improvement cycle.
1. Connect
Unify equipment and operator data in the cleanroom.
2. Analyze
AI and analytics predict drifts and pinpoint deviations.
3. Act
Automate quality workflows and flag deviations.
4. Improve
Monitor, measure and reduce release times.
5. Impact
Measurable results in eBR release, compliance and HVAC energy.
Ready to digitize your pharmaceutical operations?
Join the life-sciences leaders using CIPA to ensure compliance, maximize traceability and optimize yield. Our experts are ready to give you a tailored demo based on your real constraints.