Bioprocessing Solutions for Biopharma

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Powering productivity across biopharma workflows

Biopharma workflows encompass complex upstream and downstream steps that must progress efficiently without compromising consistency. Variability, raw material demands, and shifting timelines can slow development and complicate scale-up, whether optimizing monoclonal antibody (mAb) titers, working through vector purification, or managing messenger RNA (mRNA) yield. To help keep programs moving, biopharma bioprocessing solutions connect steps from early development through manufacturing, supporting steadier performance and fewer unplanned interruptions as teams advance toward cGMP readiness.

Connected solutions across every stage of bioprocessing

Reduce gaps as programs move from bench to production by bringing activities, such as media preparation, purification, and analytics, into a more cohesive workflow. Thermo Fisher Scientific supports this approach with solutions built to align upstream and downstream needs, enabling teams to choose options that work for both current programs and future requirements.
 

Accelerate process development and scale-up

Even well-defined early methods can exhibit different behavior at larger volumes. Changes in mixing, control strategies, or raw material characteristics often impact reproducibility as teams transition to cGMP conditions. Establishing a clear path from small-scale evaluations to manufacturing runs helps reduce this uncertainty. Our solutions and services support method development, equipment transition, and scale-up planning, enabling teams to maintain consistent performance as complexity increases.

Maintain reliability with global supply and support


Support steady access to materials, documentation, and support as teams progress toward cGMP production. Our global network is built for coordinated manufacturing and quality alignment. With consistent supply and responsive technical assistance, biopharma teams can focus on execution rather than contingency planning.

Optimize performance with bioprocessing solutions

As programs advance, process requirements tighten and expectations for documentation, control, and consistency increase. cGMP-ready technologies and services can help refine upstream and downstream processing, including cell culture strategies, purification decisions, buffer requirements, and single-use system design. This combination helps teams navigate shifting operational demands and maintain efficiency from development through manufacturing.

Bioprocessing products

Support consistent performance and steady scale-up as workflows advance toward manufacturing with Gibco media, chromatography resins, single-use systems, process liquids, and more.

Bioprocessing services

Empower workflows with services for buffer and media preparation, raw material sourcing and supply, pharmaceutical analytics, and more, to help teams address scale-up requirements and stay aligned with cGMP expectations. 

Build sustainable and scalable bioprocesses

Strengthen operational efficiency and resource management by integrating sustainable materials, energy-efficient process design, and regional manufacturing into your workflows. These actions help reduce transport impact, enhance supply continuity, and create a clearer path for long-term scalability as development expands.

Solutions across modalities and applications


Modalities, such as monoclonal antibodies (mAbs), vaccines, messenger RNA (mRNA), antibody-drug conjugates (ADCs), cell therapies, and gene therapies, often encounter different challenges as they move from early studies to scale-up. Flexible bioprocessing solutions support these varied applications, helping teams adapt methods as their pipelines expand.
 

Supporting customers that drive innovation

Productivity, consistency, and scalable development are priorities shared across the bioprocessing landscape. Thermo Fisher supports these needs across sectors, working to advance therapies. Learn more about the industries we serve.

Biotech

Comprehensive bioprocessing services and technical support help organizations optimize workflows and scale development processes. 
 

CDMO

Integrated solutions help contract development and manufacturing organizations (CDMOs) maintain consistency across client programs, support clear technology transfer, and manage scale-up with predictable performance.

Resources and insights for biotech innovators


As methods evolve, biotech teams benefit from practical, detailed guidance. Case studies, webinars, and technical notes highlight common upstream, downstream, and analytical challenges, helping teams refine decisions and prepare for later development stages.
 

Power progress in biotech workflows

 

Discover Thermo Fisher bioprocessing solutions for biotech. We offer catalog and custom services, specialist expertise, and technical support.

For research use or further manufacturing. Not for diagnostic use or direct administration into humans or animals.