Liquefied natural gas (LNG) facilities require careful pressure management on their incoming gas pipelines. In a recent LNG Industry article, Turn it Up (and Down), Emerson's Michael Calvert describes the challenges and solutions around the Santos Gladstone LNG (GLNG)...
Operations & Business Management
Optimizing Batch Process Automation Design in MES and DCS
For pharmaceutical and biotech manufacturers, the flow and capture of information is as important as the flow of the manufacturing process in readying products to release for sale. In a Pharmaceutical Technology magazine article, Connecting MES to Process Control,...
US FDA Quality Metrics Guidelines Update
Author: Eric Kuebler Since the Continued Process Verification (CPV) guidance in 2011, the U.S. Food and Drug Administration (FDA) has been talking quality and verifying process state of control. Now the FDA is getting around to defining what that looks like and what...
Conference Room Pilots to Generate Involvement in MES Projects
Author: Jonathan Lustri As a Life Sciences consultant, I get involved in many different aspects of MES [manufacturing execution system] projects. In a recent project, I helped define the project execution plan. I knew Emerson's biotech customer was highly concerned...
Reducing Communications Problems during Shift Changeovers
Sources of unplanned downtime can be many including equipment failures and human error. For downtime resulting from operator interactions, one major source of errors is the communications breakdown that sometimes happens during a shift change. If not told or seen in...
Prototype Manufacturing Operations Management Projects
The ANSI/ISA-95 standard defines models for the information flows between the instrumentation and automation layers up to the enterprise information layers for process manufacturers and producers. Moving up the levels increases the need for people, processes and...
Continued Process Verification in the Process Validation Lifecycle
In 2011, the U.S. Food and Drug Administration (FDA) issued a Guidance for Industry – Process Validation: General Principles and Practices. It highlighted a third validation stage goal of continued process verification (CPV) for: …continual assurance that the process...
RFID Tagging for Materials Movements
Some of the technologies making the Internet of Things (IoT) possible include WirelessHART, radio-frequency identification (RFID), near field communication, barcodes, QR codes and digital watermarking. I mention this because many process operations require material...
Successfully Automating Terminal Operations
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...
Improving Technology Transfer by Earlier Adoption of Standards and Software Platforms
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...
Managing Terminal Logistics
Moving and properly accounting for the products in a terminal facility requires quite a bit of logistical support and reporting. In this 14:57 YouTube video, Syncade Logistics: Reducing Product Integrity Surprises, Emerson's Brian Crandall demonstrates how these...
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The opinions expressed here are the personal opinions of the authors. Content published here is not read or approved by Emerson before it is posted and does not necessarily represent the views and opinions of Emerson.