How Baxter Met FDA Regulations With New Automation Software Installation

As a global diversified healthcare company, Baxter S.A. applies a unique combination of expertise in medical devices, pharmaceuticals and biotechnology to develop products that advance patient care worldwide. Baxter’s Lessines, Belgium facility is responsible for manufacturing single and multiple compartment storage bags for administering nutriments to patients intravenously. To streamline its operations, manage operating costs and conform to the U.S. Food and Drug Administration’s 21 CFR Part 11 compliance standards, Baxter needed to revise its manufacturing facility processes to incorporate automation methods into a new production line.