Newsletter | September 17, 2025

09.17.25 -- A Case Study In Continuous Process Verification

SPONSOR

Webinar: Expert Roundtable: Real-World Process Intensification Strategies for Smarter Biomanufacturing

Discover how leading experts are using process intensification (PI) to cut costs, boost yield, and future-proof biopharma manufacturing. In this Sartorius webinar, gain practical insights on modernizing legacy facilities, implementing PI across upstream and downstream, and leveraging automation, digital tools, and modular upgrades. See real-world case studies proving how to deliver more—without building more. Click here to learn more.

FOCUS ON FILL-FINISH

Unlock The Power Of Biophysical Tools In Biotherapeutic Development

Unlock innovation in biotherapeutics with expert insights into DSC and molecular stability. Learn how biophysical techniques can optimize formulations and enhance nucleic acid stability.

Navigating Your Holistic Approach To CCI For Biologic Drug Products

Explore regulatory framework and expectations, and see the benefit of a comprehensive approach to CCI tailored for mAbs and complex modalities such as fusion proteins or bioconjugates.

Fluid Connection Technologies For Sterile Fill and Finish Process Design

Single-use technology and innovative fluid connections play a significant role in creating an effective, sterile fill and finish operation that maintains the integrity of your biologic products.

FILL-FINISH SOLUTIONS

Flexible Filling Capabilities For Rigorous Demands - Argonaut Manufacturing Services

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Webinar: Streamlining Vaccine Purification: Techniques for Modern Modalities

Advances in vaccine development demand faster, more efficient processes. This Thermo Fisher Scientific webinar explores chromatography purification tools that accelerate downstream development for diverse vaccine modalities, including mRNA, viral vectors, recombinant proteins, and VLPs. Through case studies on HPV, Malaria, and COVID-19, attendees will learn how affinity and ion exchange resins enable high-purity, high-yield purification from lab to large-scale production. Click here to learn more.

FOCUS ON DOWNSTREAM MANUFACTURING

A Case Study In Continuous Process Verification

CPV can strengthen the bridge between compliance and continuous improvement. In this scenario, a hypothetical lab sets out to improve process yields and efficiency.

Sterile Gas Filtration And Optimization In Bioprocessing

Unlock insights into sterile gas filtration challenges in bioprocessing. Watch this on-demand session to learn optimization strategies for critical applications and improved filter performance.

Bridging Anti-E. coli HCP Antibodies And E. coli Antigens

Read this expert comparative coverage analysis study performed to assess the reactivity of anti-E. coli HCP antibodies that support ELISA kits.

Demand More From Your Oligo Synthesizer

The market for oligonucleotide therapeutics is expanding, and the pipeline is diverse. Gain insight into how you can fast-track your molecule's development with verified synthesizers, columns, and scientific support and expertise.

Optimize mAb Purification Using Protein A Membrane Chromatography

Discover how high throughput (HTP) screening can utilize membrane chromatography at comparable consumables costs to traditional resins without compromising CQAs for prescribed therapeutics.

Scalable Process Solution For EV Purification With 10X Yield Improvements

Biological components in conditioned media are a consistent problem during downstream processing of EVs. A novel in-process reagent prevents these issues and improves particle recovery 10-fold while maintaining CQAs.

Innovative Therapeutic Applications Of Ion Exchange Resins

Chromatography resins are aiding in the delivery of cancer and inflammatory disease therapies. Learn how ion exchange resins act as therapeutic carriers for advanced drug delivery.

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Webinar: Filtration unfiltered: Technology to meet new bioprocessing challenges

Join Cytiva experts as they reveal how to overcome filtration challenges in today’s evolving biopharma landscape. Discover how process intensification drives efficiency, explore strategies for managing diverse drug modalities, and gain insights into key regulatory considerations—including PUPSIT and PFAS. Don’t miss this opportunity to learn how smarter filtration solutions can boost productivity and support sustainable bioprocessing. Click here to learn more.

DOWNSTREAM MANUFACTURING SOLUTIONS

The Ultimate Solution For Your Chromatographic Separations - Waters Corporation

Pre-Use Post Sterilization Integrity Testing (PUPSIT) Overview - Cytiva

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