Newsletter | August 12, 2026

08.12.26 -- Using Better Tools And Better Data To Drive Process Productivity

SPONSOR

Webinar: Controlling UF/DF with Confidence: How to Define, Monitor, and Hit Critical Endpoints

UF/DF may seem straightforward, but endpoint selection and process control often determine scalability and consistency. Join Repligen to learn practical strategies for defining critical concentration and diafiltration endpoints, leveraging real-time in-line analytics, reducing manual intervention, and minimizing variability across scales. Gain actionable insights to improve reproducibility, streamline tech transfer, and strengthen manufacturing performance. Click here to learn more.

FOCUS ON DOWNSTREAM MANUFACTURING

Using Better Tools And Better Data To Drive Process Productivity

In this segment from the Bioprocess Online Live event, “The Levers And Tradeoffs That Drive Process Productivity,” our panelists respond to an audience poll and answer audience questions about hollow fiber membranes and process modeling approaches. They agree that productivity gains emerge from a comprehensive understanding of the process and the tools that enable it.

Inline Buffer Formulation: A Facility Operations Game Changer

Inline buffer formulation leverages real-time, precise buffer preparation throughout production, enabling agile, efficient, and scalable manufacturing processes that save time and resources.

Pushing The Boundaries Of Chromatographic Separation

Metal-sensitive analytes often suffer from poor recovery and distorted peak shapes. Explore how inert hardware improves sensitivity and chromatographic performance for challenging analyses.

Product-Wet Integrity Testing: Risk-Based Strategies

When standard water‑based integrity testing falls short, product‑wet approaches can offer a more representative alternative. Learn how risk‑based strategies are used to establish reliable test limits.

Development Of Scalable Purification For Biotherapeutic Peptides

Discover key strategies for reversed-phase isolation of biotherapeutic peptides, as well as method development, scale-up techniques, and RP/MS analysis to enhance purification workflows.

The Hitchhiker's Guide To Creating Oligonucleotides From Start To Finish

Producing high-quality oligonucleotides requires precise execution across multiple stages. Gain a clearer understanding of the mid-scale production workflow and necessary quality control measures.

Innovative Therapeutic Applications Of Ion Exchange Resins

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

A Faster And More Economical Path To Investigational New Drug Applications

Read how new membrane-based protein A affinity chromatography technology can greatly shorten the time it takes to get to IND while also making the process less expensive and more adaptable.

Evaluating Antibody Fragment Purification Using VH3 Resin

Find out how VH-domain targeting enables efficient purification of VH3 antibody fragments and bispecific formats, with strong recoveries and flexible wash conditions that support improved purity.

DOWNSTREAM MANUFACTURING SOLUTIONS

Multitools For Clarification And Harvest - CARR Biosystems

Modifying Elution Conditions For Enhanced Impurity Removal - Ecolab, Purolite™ Resins

Effective Nucleic Acid Removal In High-Salt, GMP Workflows - QIAGEN

SPONSOR

Webinar: Enabling the full potential of process chromatography

Scaling purification processes without sacrificing performance is a major challenge in biomanufacturing. Join Repligen to discover how advanced process control, real-time analytics, and integrated PAT can improve chromatography performance, maintain critical quality attributes, optimize resin utilization, and support confident scale-up from process development through GMP manufacturing. Register today to learn practical strategies from industry experts and enhance manufacturing efficiency. Click here to learn more.

FOCUS ON FILL-FINISH

Predicting Performance Of Lotions Through Rheological Characterization

Rheological testing shows how small formulation differences influence spreading. With minimal sample volumes, these methods connect lab measurements to real‑world performance.

Developing Non-PEG Stabilizer Lipids For Nucleic Acid Lipid Nanoparticles

Non-PEG stabilizer lipids may offer a new path for LNP design. Combining strong colloidal performance with greater chemical flexibility helps address growing concerns around PEG-related immunogenicity.

Implementing High-Volume Drug Handling And Packaging Programs

Simplify the complexity of combination product development by partnering for integrated support across device design, industrialization, manufacturing, and final product assembly.

The Case For Modernizing Small-Volume Aseptic Processing

Tube welding and biosafety cabinets present significant costs and risks for small-volume aseptic processing. Modern single-use aseptic connectors offer a more efficient alternative.

FILL-FINISH SOLUTIONS

Atmos Isolator For Fill/Finish Applications - AST

Drug Product Fill And Finish - Curia

Connect With Bioprocess Online: