There are many ways to optimize or intensify a process – so how do you know which approaches are worth pursuing for your process? This webinar is a good s...

Whether you're looking to scale up or optimize a process, equipment reliability and flexibility can make a huge impact on your costs and timelines. In this...

Cytiva helps biopharma companies worldwide develop advanced medicines. In this interview, Emmanuel Abate, President of Genomic Medicine and Head of Sustain...

Join Thibault Renaud, Sustainability Supply Chain Leader at Cytiva, and Rachel Delacour, CEO and Cofounder of SWEEP, as they dive into the crucial role of ...

Tune into our discussion with Ryan Walker, Senior Director of Sustainability at Cytiva, and Aude Arkam, Global Head of Eco Design & Circular Economy at San...

Traditional process liquid and buffer manufacturing has been shown to be resource-intensive, in both facility footprint and labor costs, as the production ...

As the trend towards subcutaneous drug administration grows and drug formulations become more concentrated, careful consideration is required when selectin...

The Cytiva Security of Supply program applies a data-driven approach to identify and reduce supply chain risk. It encompasses business continuity managemen...

Improving usability, efficiency, and reliability were our focus when we designed the new ÄKTA process™ chromatography system. In this virtual workshop, you...

In this session, an introduction to DoE and examples of different experimental designs is covered.

Simulation for in silico process development is becoming a viable option to reduce the time needed for chemicals, manufacturing, and control (CMC) activiti...

When improving biopharmaceutical process development, mathematical models play a crucial role, especially to generate enhanced process understanding and to...

At Cytiva, we are committed to supporting your path to scientific breakthroughs. For over 200 years, our innovative solutions have guided scientists throug...

Watch our discussion on the expanding field of targeted protein degradation and the technologies used to characterize these unique molecules. In this emerg...

Robust and reproducible analytical method for product development and quality control

Introducing new Cytiva™ Protein Select™ resin - For recombinant protein purification in research and process development By Emma Lind, Product Manager at ...

Since the FDA approved the first monoclonal based therapy in 1985, mAbs have had significant clinical success and have been used to provide effective treat...

As regulations become more stringent, microbiological testing and analyses are critical to ensure the quality of pharmaceutical products. The membrane filt...

Automate your impurity ELISA testing using Cytiva Impurity ELISA kits and Beckman Biomek i5 liquid handling systems.

This video describes how to set up and run a method for Biacore Single-Cycle Kinetics (SCK)™.

This video describes how to import sample information when setting up a run method in Biacore™ Insight Control Software.

This video describes how to convert methods from Biacore™ 1 series to Biacore™ 8 series SPR systems.

This video describes how to load samples and reagents into your Biacore™ 8 series instrument.

This video describes functionality of Biacore™ Insight Control Software that you can use to quickly assess your ongoing or completed runs.

CAR T therapies are gaining increased attention due to their demonstrated potential in patient outcomes. For a successful commercialization of these therap...

Reduce operator-derived errors with the help of Sefia™ platform. Keep an eye on how everything is going: the system’s functionally closed design and automa...

According to data from our 2023 Global Biopharma Resilience Index, 55% of pharma leaders are happy with the speed of drug approvals — meaning 45% feel ther...

Learn all about Fast Trak™ services from Cytiva from our very own Fast Trak™ Global Technical Leader, Sabrina Carmichael. In this video, you’ll get an over...

The separation of adeno-associated virus (AAV) with high yield and purity is an increasingly important challenge. Mechanistic modeling is the tool of choic...

As cell therapy rapidly progresses, tumor infiltrating lymphocyte (TIL) therapies are playing a significant role in shaping the field. What milestones ena...

In this webinar, we’ll discuss our journey in becoming the first GMP-certified cell and gene therapy manufacturing facility in Thailand. During the journey...

Learn more about the latest addition to our family of single use chromatography systems and how this will enable you to better purify small volumes in a GM...

In the early clinical development stage of autologous cell therapy manufacture, labor costs often dominate the overall cost of goods sold. However, as manu...

As a major supplier for cell and gene therapy manufacturers, Cytiva continuously strives to advance and accelerate new therapeutics by bringing innovative ...

Enriching mononuclear cells (MNCs) by removing other cell types and contaminants is a critical step in CAR T cell therapy production. But do you know why, ...

Manual cell expansion: variable and prone to errors. Especially when multiple operators are involved. One solution? Automation, which can improve the repro...

For decades, PCR has been the gold standard for detecting specific DNA and RNA sequences. However, PCR is limited in its accessibility for rapid on-site te...

Join our webinar to learn how blood separation steps improve point-of-care tests (POCT) like lateral flow assays (LFA), enhancing accuracy and reducing pre...

Commercially available antibodies are typically poorly characterized and supplier statements on intended use are not necessarily reliable. Surface plasmon...

The fiber pads you use in your lateral flow assays can affect performance and results. Choosing the right fiber pad can ensure test-to-test reproducibility...

Novel therapeutics are bursting onto the scene at a rapid rate as innovators race to harness the power of mRNA, cell therapies, and other gene-based treatm...

Advances in molecular and immunodiagnostics are enabling a personalized, high-precision approach to health in many clinical areas. But how will this conti...

Join Linda Mathiasson, Strategic Customer Leader for Nucleic Acid Therapeutics at Cytiva, to look at the history of mRNA immunotherapy, cancer vaccine mod...

Take a deep dive into nitrocellulose membranes including the raw material, structure manufacturing process and capillary flow time and how these affect you...

When selecting materials for immunoassay development, membrane properties, and reagent properties must be considered together, as their interactions determ...

Advances in molecular and immunodiagnostics are enabling a personalized, high-precision approach to health in many clinical areas. Customized contract man...

Today, researchers can analyze 10 000+ cells from one tissue sample or patient to understand individual cell populations and their behaviour in diseased ti...

Join our webinar hosted by Monika Seidel (PhD) to discuss the results of a study using Cytiva’s magnetic silica bead-based Sera-Xtracta™ Cell-Free DNA extr...

Biopharmaceutical impurities such as host cell proteins can delay biologics development and production. These elements can have immunogenic effects in pati...

The second of a two-part qualification webinar series continues our look at qualification services as it relates to the continued lifecycle of a Cytiva ins...

Proper care and maintenance of your ÄKTA chromatography system is essential to ensure optimal performance. Failure to maintain your system can lead to poor...

Your bioprocess operation is critical. An unplanned breakdown can negatively impact your batch production schedule and ability to provide critical medicine...

Employing the proper care and storage procedures can keep your Biacore system operating trouble free. The material presented will show you how to take your...

Proper routine care procedures, calibration verification, and basic troubleshooting are critical to ensuring your WAVE/Xuri 25 system operates in peak cond...

This webinar covers a detailed walkthrough of the Biacore Insight Evaluation Software eLicense activation and license configuration process. This versatile...

A two-part webinar series providing a basic understanding of qualification services concepts and terminology used when operating in a GxP environment with ...

What are the most important details to consider when designing a purification protocol? From chromatography techniques to system choice, we will guide you ...

This webinar will discuss the properties to consider when selecting a hydrophobic filter membrane for specific market applications. Additionally, you will ...

Conociendo el agente causal y sus vías de transmisión para una correcta implementación de las políticas de salud pública

Learn more about the performance of Pall's Vivid™ Lateral Flow Nitrocellulose Membrane.