Life Sciences Drug Manufacturing Facility Layout

Ensuring drug safety and efficacy across the life sciences value chain​

From upstream to downstream drug manufacturing, Emerson offers innovative solutions to help you stay ahead of the evolving life sciences industry. These cutting-edge technologies are designed to meet the growing demands of your operations by enhancing productivity, reducing costs, and accelerating time-to-market.​

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Solutions in Action: Measurement Instrumentation for Upstream Drug Manufacturing​

Buffer and media preparation are essential in the drug manufacturing process, as these components provide the necessary environment needed for growth (USP) and purification (DSP) steps. By utilizing advanced measurement technology, manufacturers can effectively tackle variability issues, maintain stringent quality standards, and streamline operations. Process instrumentation enhances overall productivity allowing manufacturers to consistently produce high-quality products. 

Solutions in Action: Measurement Instrumentation for Downstream Drug Manufacturing​

Effective chromatography operations ensure reliable and consistent separation, purification, and analysis of complex mixtures, vital for maintaining product quality and operational efficiency. By leveraging advanced measurement and control solutions, manufacturers can optimize their chromatographic processes, ensuring high-quality outputs, minimizing contamination risks, and ultimately accelerating the pace of new drug therapies. 

Direct flow filtration (DFF), also known as dead-end filtration, is a crucial technique for efficiently removing solid contaminants from liquid products. Integrating accurate and reliable measurement tools is crucial for maintaining consistent filtration performance, optimizing throughput, and minimizing product loss. By providing precise monitoring and detailed process insights, advanced measurement instrumentation enables manufacturers to fine-tune their processes, uphold high-quality standards, and meet regulatory requirements, leading to safer and more effective drug products.

Tangential flow filtration (TFF), also known as crossflow filtration, is an integral technique for various stages of drug production to ensure high-purity products by efficiently separating and purifying biomolecules. The efficiency and consistency of TFF greatly depend on having accurate and reliable measurement instrumentation to maintain precise process control, monitor key parameters, and ensure optimal filtration performance, thereby enhancing product quality and compliance with regulatory standards. 

Solutions in Action: Measurement Instrumentation for Utilities​

Ensuring the efficacy of clean-in-place (CIP) and steam-in-place (SIP) systems is vital for preventing cross-contamination, maintaining high safety standards, and achieving batch-to-batch consistency. Drug manufacturers must rigorously implement and monitor these systems to adhere to regulatory requirements and industry best practices. Precise measurement instrumentation can aid producers in verifying the effectiveness of cleaning processes to ensure the overall safety and integrity of the final drug product. 

As energy costs rise, efficient energy management strategies are crucial to identify inefficiencies, reduce consumption, and lower operational expenses. Advanced monitoring and control systems allow for data-driven decisions that further enhance productivity and environmental sustainability. This increased visibility into energy distribution and consumption patterns enables targeted improvements to optimize overall energy usage. 

Clean compressed air is often costly due to the need for high-quality filtration systems to maintain quality and purity standards. Integrating precise measurement and automation solutions allows drug manufacturers to gather detailed consumption data, identify leaks, and optimize their compressed air systems for improved sustainability and operational efficiency. 

Frequently Asked Questions About Measurement Instrumentation for the Life Sciences Industry

Why are reliable measurement instruments so important in the drug manufacturing process?
What constitutes reliable measurement instrumentation?
What are examples used today to translate instrument data for improved process control, robust diagnostics, and regulatory compliance?
Where is the future of instrumentation heading in the world of drug manufacturing?
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