PMO helps users with 21CFR compliance

Rockwell Automation's Pharmaceutical Manufacturing Optimization (PMO) solution is reported to help companies reduce drug manufacturing costs, increase efficiency, improve time-to-market, and comply with government regulations, such as 21CFR Part 11, ''Electronic Records and Signatures.''

By Control Engineering Staff January 1, 2002

Milwaukee, WI – Rockwell Automation’s Pharmaceutical Manufacturing Optimization (PMO) solution is reported to help companies reduce drug manufacturing costs, increase efficiency, improve time-to-market, and comply with government regulations, such as 21CFR Part 11, ”Electronic Records and Signatures.” PMO solutions consist of consulting services and standardized software templates customized to integrate manual interventions with automated batch operations, including tracking and recording product genealogy, batch lots, in-process material, product quality, production analysis, asset utilization, and capacity scheduling.

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