How CIPA is transforming the cosmetics & medical device industry
Manufacturing medical devices and cosmetics demands operational rigor and full traceability. CIPA provides a complete digital platform to standardize your sterile cleanroom operations.
From raw syringe or implant components to the final sterile seal, CIPA helps manufacturers guarantee ISO and FDA compliance, speed up release and manage efficiency.
4 ways CIPA strengthens cosmetics & medical device operations
Browse the cards to explore each lever: the data, the visuals and the before/after CIPA comparisons.
Strengthen ISO 13485 & 22716 regulatory compliance
Meet the strict requirements of ISO 13485 (medical devices) and ISO 22716 (cosmetics GMP). Follow FDA requirements (21 CFR Part 820) by centralizing and tracing execution data.
- Complex manual preparation for ISO/FDA audits
- High risk of missing paper documentation
- Disconnected tracking of non-conformities and CAPA
- Audit trail hard to rebuild on the spot
- Instant readiness for ISO and FDA audits
- Complete, tamper-proof digital audit trail
- Automated management of deviations and CAPA plans
- Documentation that meets medical-grade standards
DMR file approval
ISO 13485 control plan approved
Cleanroom line inspection
Sterile pouch seal validation in progress
Dual signature & release
Batch release report generated
3 ways CIPA accelerates product quality, 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 the industrial transfer of your cosmetic formulas or medical device designs to mass production lines by centralizing your recipes.
- R&D-to-engineering recipe transfer on paper
- Scale-up that is hard to document
- Slow, rigid new product introduction (NPI)
- Errors when adapting formulations for production
- Centralized repository of standard digital recipes
- Live collaboration between R&D, quality and engineering
- Scale-up documented step by step
- Dramatically shorter time-to-market
One platform for quality, traceability and ISO compliance.
CIPA unifies people, processes and data to deliver connected insights across the value chain — ISO 13485 and ISO 22716 GMP compliance, sterile cleanroom eBR, UDI serialization and automated audits.
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 scrap.
3. Act
Automate quality workflows and manage deviations.
4. Improve
Monitor, measure and optimize cycle times.
5. Impact
Measurable results in batch release, compliance and energy.
Ready to digitize your cosmetics & MD operations?
Join the industry leaders using CIPA to ensure compliance, maximize traceability and optimize OEE. Our experts are ready to give you a tailored demo based on your real constraints.