Pharmaceutical and biotech manufacturers seek to improve both project and operational performance through implementation of smart factory technology. The smart factory fits right into the S95 enterprise automation model and provides out-of-box manufacturing functionality representing the best practice in the industry and complying with the regulation such as cGMP. The smart factory technology connects the […]
Pharmaceutical and biotech manufacturers have stringent regulatory compliance requirements. These requirements must balance with the need for improvement and optimization to run safely, efficiently, profitably and in line with the business and quality objectives. In a Pharma Bio World article, The Crossroads of Compliance, Audit Readiness, Profitability, and Data Integrity, Emerson’s Michalle Adkins opens: True […]
Making an operational step change in a production process involves a clear vision and people, processes and tools to execute the vision. A July/August 2014 Tank Storage magazine article, Automating terminal operations, highlights the story of Vopak transforming their operations from remote manual to fully integrated. Emerson’s Cor Vermeijs and Chris Amstutz collaborated with Vopak’s […]
The Emerson Exchange conference October 6-10 in Orlando, Florida USA is rapidly approaching. I caught up with Emerson’s Michalle Adkins who mentioned that her team of Life Sciences consultants would be highlighting the enablement of release by exception. Although release by exception and real-time release are not yet a reality for the majority of pharmaceutical […]
In 2011, the U.S. Food & Drug Administration (FDA) published their Guidance for Industry – Process Validation: General Principles and Practices. A PharmManufacturing.com article, A Framework for Technology Transfer to Satisfy the Requirements of the New Process Validation Guidance: Part 2 shared the impact on the Life Sciences industry: In the life of any drug […]
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