Newsletter | August 6, 2026

08.06.26 -- Bridging The Gap Between Vaccine Platforms And CDMO Economics

SPONSOR

Webinar: When Unexpected Particles Threaten Your Biologic

Discover how advanced particle forensics can help resolve unexpected particle findings with confidence. In this webinar, KBI Biopharma experts explain how clinical in-use studies and techniques including Raman, FTIR-ATR, and SEM-EDS identify particle sources, assess risk, and generate regulator-ready evidence. Learn practical strategies to accelerate investigations, protect product quality, support patient safety, strengthen development decisions, and streamline regulatory submissions efficiently. Click here to learn more.

INDUSTRY INSIGHTS

Mirror, Mirror Makes RNA-Targeted Discovery Smarter

Examine a mirror‑image screening approach that eliminates DNA:RNA hybridization, revealing true binders and unlocking clearer, more productive DEL results for challenging RNA targets.

A Look At The Evolution Of Aseptic Manufacturing

The transition toward complex biologics and patient-centric delivery is redefining sterile manufacturing. Success now depends on adopting flexible production strategies and advanced technologies.

Prefiltration And Sterilizing Filtration Of Plasma Based Products

Layered filtration reduces particles and microbes at each stage, protecting filters, improving reliability, and ensuring consistent, high-quality output.

FEATURED EDITORIAL

Bridging The Gap Between Vaccine Platforms And CDMO Economics

Can a biotech create a CDMO market? GeoVax, an infectious disease/oncology biotech, may have just done so. David Dodd, CEO, believes we should all concentrate more on whether the outsourcing model can align with evolving technology platforms. Both sponsors and CDMOs may need to change things up.

Control, Cost, And Capability: Making Smarter Outsourcing Decisions

Here's a case for the biotech hybrid model, one that relies on a crack team of internal core talent complemented by broad reliance on external vendors.

INDUSTRY INSIGHTS CONTINUED

The Benefits Of Transparent Pricing

Streamline biopharma budgeting and expose hidden contract manufacturing fees. An all-inclusive pricing model ensures predictable partnerships from initial scale-up to commercial approval.

Mammalian Expression

See how a biotechnology company advanced an engineered protein therapeutic while navigating development, regulatory, and scalability challenges. 

The Growing Strategic Role Of Analytical Laboratories

Analytical labs are becoming strategic partners, enabling faster decisions, integrated expertise, and stronger collaboration across development, manufacturing, and quality.

How We Deliver The Promise Of CDMO Partnership For Biotechs

Development partnerships start with early alignment, transparency, and shared accountability, reducing risk, improving scalability, and supporting success as programs advance.

Moving Beyond Known Targets

A pioneering perspective explores how new scientific thinking, physics‑based insights, and bold leadership are expanding the druggable universe and opening therapeutic paths.

Accelerating Freeze-Drying With Ice Nucleation

Assimilate how controlled ice nucleation shortens lyophilization cycles, supports higher drying temperatures, and reduces complexity for amorphous and mixed formulations without sacrificing quality.

How Integrated Data Systems Enhance Clinical Development

Delve into how cloud-based systems and unified data platforms are transforming biomanufacturing by enhancing efficiency, ensuring quality, and accelerating the delivery of complex therapies to market.

De-Risking A Bioconjugate's Development Path From Discovery To Clinic

Understanding the obstacles you may face during bioconjugate development, as well as the tools available to help overcome them, can help streamline your product’s path to market.

3 Keys To Rare Disease Clinical, Commercial Drug Product Manufacturing

The complex biology of rare diseases creates unique hurdles, making it difficult to design and implement a drug development program. Explore the unique considerations for drug product manufacturing.

SOLUTIONS

Simplifying ADC Development Through CDMO Collaboration

The Future Of Large-Molecule Manufacturing

Driving Innovation In Fill/Finish And Lyophilization

Two Decades Of Sterile Manufacturing Excellence

Leveraging Advanced Tech, Proven Expertise From Cell Line Development

OUTSOURCED PHARMA CAPABILITIES UPDATE

Find Your New CDMO At Outsourced Pharma Capabilities Update

CDMOs in biologics, cell and gene, and small molecule share their capabilities and available capabilities. See for yourself why this virtual event has become a wildly popular resource to identify options for your development and manufacturing needs.

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