Baxter S.A.

AVEVA has enabled the BiiON engineers to create roughly 35 reusable generic objects, which are stored in a central library

Baxter S.A.

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.

Goals

  • 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

Challenges

  • 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

Results

  • 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

"To be successful, strategic projects require excellent collaboration between the customer, the software vendor, and integrator. By establishing the automation framework, AVEVA software enabled our project teams to focus on productivity targets."

– Serge Bassem, CEO

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