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Succeed with customized support plans offering the right ingredients

Designing service solutions begins with your success goals in mind. We build your plan to ensure all the right elements are in place for productivity and compliance, including risk management solutions to help you minimize unexpected downtime and keep things running smoothly. We even help you empower your team to confidently manage your Cytiva equipment.

Optimize your uptime with strategic consulting spare parts advisory service

Stay confident that you have the right parts when you need them. Our spare parts advisory service is a data-driven approach to support your risk-based decisions. Our analysis considers the number of systems at your facility, manufacturing process criticality, frequency of equipment use, component criticality, type of wear, and other variables. We’ll help you keep only the parts you need and in the appropriate quantity to stay lean and sustainable.

Maintain your Cytiva equipment’s qualified state

Embark on your GMP manufacturing journey with our qualification knowledge by your side.
Rely on our dependable IQ/OQ protocols for compliance with regulatory standards. When your equipment is repaired, relocated, upgraded, or modified, Cytiva can help you keep it in a qualified state with requalification and change control procedure services. Improve audit preparation, navigation, and audit trail, and reduce errors through e-Qualification with ValGenesis software.

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Sed feugiat libero eu turpis tincidunt iaculis. In vel aliquam est, at porta neque. Donec hendrerit ultrices consectetur. Integer feugiat massa quis arcu ullamcorper, tristique facilisis massa feugiat. Phasellus risus mauris, pretium vitae tortor non, tristique fringilla tortor. Aliquam volutpat eros ac risus consectetur, quis gravida erat lobortis. Quisque id rutrum enim, sed fermentum nisl. Nulla volutpat turpis ac ligula venenatis maximus. In non dui ante. Sed ullamcorper quis nisi.

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ELEVECTA™ transient cell line

Preseves flexibility while delivering excellent performance and quality - all aimed at quickly advancing candidates to clinical trials.

• Excellent performance: Achieve high titers of infectious virus, which you can boost further by using enhancers.
• Enhanced product quality*: Minimize DNase-resistant host cell DNA inside capsids.
• Innovative: Access advances in cell line engineering across the entire portfolio to support transition between cell lines.
• Collaborative: Benefit from a comprehensive suite of regulatory support services.

ELEVECTA™ packaging cell line

Contains all genes except the transgene; allows streamlining the screaning of assets that use the same capsid to target the same tissue type.

• Streamlined screening: Efficiently screen multiple assets that target the same tissue type.
• Cost-effective approach: Reduce your plasmid costs with single-plasmid transfection compared with triple transfection.
• One cell line to clinic: Go to clinic with one cell line and simplify your regulatory asks when you’re targeting the same tissue type across your programs.

ELEVECTA™ producer cell line

Contains all genes to produce AAV; simply induce. The result is a simplified, robust, upstream process that easily scales to treat hundreds of thousands.

• Simplified manufacturing process: Replace multi-step transfection with one-step induction.
• Easy scalability: Scale up seamlessly to achieve large quantities of AAV material.
• Enhanced reproducibility: Produce AAV from a monoclonal cell line, enabling batch-to-batch consistency.
• Reduced COGS: Skip the need for transfection reagent and any plasmid DNA, which are the most expensive raw materials.