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Blood Plasma Processing Systems

Engineering process systems for plasma fractionation and purification.
Integrated technologies enabling efficient, GMP-compliant production of plasma-derived therapies.
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Clearnroom view with large filter press
Filter press for filtration of the precipitate.

Transforming blood plasma. Into life-saving therapies.

Plasma-derived medicines such as immunoglobulins, albumin, and clotting factors depend on carefully controlled fractionation processes. These operations require precise temperature control, reliable purification strategies, and strict adherence to GMP standards throughout production.

ZETA supports plasma fractionation facilities with engineered process systems designed to maintain product integrity while improving operational efficiency. By combining process engineering, automation, and specialized equipment, we help manufacturers reliably isolate and purify therapeutic proteins from human plasma.

Conquering the challenges of plasma fractionation. Critical prerequisites for reliable production.

Batch-To-Batch Consistency

Stable operating conditions ensure consistent separation and purification performance across every production cycle.

Operational Efficiency

Optimized process design reduces infrastructure requirements and improves facility throughput.

Protein Recovery and Yield

Carefully engineered purification strategies maximize recovery of valuable plasma proteins while minimizing losses.

Low-Temperature Integrity

Controlled freezing, thawing, and cold-chain handling protect temperature-sensitive proteins throughout processing.

Regulatory Compliance

Validated systems, documentation practices, and process controls support compliance with strict GMP expectations.

Process Safety and Cleanroom Operation

Integrated safeguards protect product integrity while maintaining safe and contamination-free operating environments.

End-to-end expertise for plasma processing.

ZETA delivers integrated engineering and process solutions designed specifically for plasma fractionation facilities. Our technologies support critical processing steps while improving reliability, scalability, and regulatory alignment.

Cryogenic storage solutions

Systems for controlled freezing and storage that preserve the stability of valuable plasma fractions.

Modular cleanroom construction

Flexible cleanroom environments are designed for GMP-compliant plasma processing operations.

Process optimization & automation

Automation and digital process monitoring stabilize production conditions while improving efficiency and yield.

The image shows two pieces of industrial equipment made of shiny metal. One is a control unit with a screen and buttons, including an emergency stop. The other is a large tank with pipes and valves. Both are labeled “ZETA” and used in clean, precise manufacturing settings. A person in full protective gear—suit, gloves, and mask—is using a touchscreen on the wall in a clean, sterile room. The space contains large stainless steel machines, likely used in pharmaceutical or biotech manufacturing. Person in cleanroom clothing operating a touchscreen in cleanroom wall

Process systems for plasma fractionation. Built for stability and high‑volume.

Plasma fractionation requires tightly integrated process systems designed to handle temperature-sensitive materials while maintaining strict process control. ZETA supports these facilities with technologies such as:

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Freeze and thaw systems for plasma handling

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Buffer preparation and inline conditioning systems

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Filtration and purification systems

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Media and reagent preparation skids

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Automated process control platforms

Rethinking plasma fractionation. Engineered for reliability and efficiency.

Protect product quality

Maintain stable processing conditions that safeguard sensitive plasma proteins throughout production.

Improve operational efficiency

Optimize facility infrastructure and process workflows to increase throughput and reduce operating costs.

Maintain regulatory readiness

Implement validated systems and documentation practices aligned with global GMP requirements.

Selected Project Experience

Explore how ZETA supports complex biopharmaceutical manufacturing projects through integrated engineering, modular process systems, automation, and coordinated project execution across upstream and downstream operations.

Mobile production skids in cleanroom area, docked on their docking stations on the wall

Multipurpose Pilot Plant for Plasma Processing

High flexibility for over 30 blood plasma-derived products.

Fully automated multiproduct system covering clinical and routine production of new products in addition to pilot production. Allowing production 24/7.

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Holistic Simulation Throughout Facility Design

ZETA delivers ‘First-Time-Right’ integrated engineering using simulation.

A realistic simulation environment is capable of modeling complex batch processes with all their dependencies: utilities, cleaning systems, buffer logistics, WFI generation and more.

Improve Yield and Process Consistency Across Plasma Fractionation

Learn how ZETA’s integrated process systems can help improve protein recovery, stabilize fractionation workflows, and support efficient plasma processing operations.
The image shows three large stainless steel tanks on a platform, connected by a network of pipes and valves. It’s part of a clean, high-tech industrial system, likely used in pharmaceutical, chemical, or food production. The brand “ZETA” is visible on the left side.

Inline Buffer Conditioning for Plasma Processing

Buffer preparation plays an essential role in precipitation and purification steps within plasma fractionation facilities. Conventional buffer preparation can require significant storage capacity and complex logistics.

ZETA InFlow enables on-demand buffer inline conditioning, allowing buffers to be produced directly at the point of use. This approach reduces infrastructure requirements while improving operational flexibility and process control.

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