Posts Tagged ‘manufacturing execution system’

Manufacturing Execution Systems in Drug Research and Development

Posted in Life Sciences & Medical, Operations & Business Management on Wednesday, February 13th, 2019. No comments yet
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The U.S. Food & Drug Administration (FDA) outlines the drug development process in five steps: Discovery and development Preclinical research Clinical trials FDA review FDA post-market safety monitoring I caught up with Emerson’s Zuwei Jin whom you may recall from earlier posts on the role of automation in the drug development process. Zuwei explained to […]

Tracking Cell Therapy Chain of Identity

Posted in Life Sciences & Medical, Operations & Business Management on Monday, November 5th, 2018. No comments yet
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In this 2:25 YouTube video, Address Cell Therapy Batch Production Challenges with Syncade, Emerson’s Michalle Adkins shares how operations management technology plays an important role in addressing these challenges.

Best Practices for Implementing a Process Control Driven MES System

Posted in Life Sciences & Medical, Operations & Business Management on Tuesday, August 21st, 2018. No comments yet
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Author: Jonathan Lustri I have previously been interviewed and written about a process control and MES [Manufacturing Execution Systems] architecture where the batch control logic within the process control system is the single procedural engine. It drives procedural logic and workflows executed by the MES system when called by the process control system. The benefit […]

Moving to Electronic Batch Records

Posted in Life Sciences & Medical, Operations & Business Management on Wednesday, May 30th, 2018. One comment so far
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Yesterday we highlighted advancements in exception management technology for pharmaceutical and biopharmaceutical manufacturers. Exception management is one element in an electronic batch record (EBR). Other elements for the EBR which also have high data integrity requirements include equipment management, material management and batch record process flow and recipe management. In a PharmTech article, Making the […]

Improving Batch Manufacturing Quality Review Cycle Time

Posted in Life Sciences & Medical, Operations & Business Management on Tuesday, May 29th, 2018. One comment so far
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Exceptions in batch manufacturing processes are the deviations that occur outside the prescribed specifications. For pharmaceutical and biopharmaceutical manufacturers, quality and manufacturing personnel must review these exceptions. Traditionally, this quality review process occurs after the batch has completed. A recent news release, Emerson Helps Life Sciences Companies Reduce Time to Market with Faster Quality Reviews, […]