Baxter S.A. deployed AVEVA software to upgrade its patient care product manufacturing systems to streamline operations, as well as meet U.S. and European regulations.
- Increasing production capacity while significantly reducing manufacturing throughput time was a top priority for Baxter
- The new automation system needed to assist Baxter in achieving U.S. Food and Drug Administration FDA 21 CFR Part 11 compliance regulations
- The automation system selected for the new Baxter production line had to be fully compatible with Baxter’s existing architecture and systems
- The company required that the new system integrate Profibus-connected smart sensors into the new manufacturing line process
- Production management had to be centralised and include reporting, analysis, traceability, and performance monitoring to adhere to FDA 21 CFR Part 11 regulations, as well as European compliance standards
- The implementation of the new AVEVA system doubled the manufacturing facility’s productivity
- Baxter’s manufacturing processes are now fully traceable and meet all FDA and European regulations
- AVEVA has enabled the BiiON engineers to create roughly 35 reusable generic objects, which are stored in a central library
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