Newsletter | January 22, 2026

01.22.26 -- Metrics, Not Audits, Should Lead Vendor Accountability

FOCUS ON OUTSOURCING

Metrics, Not Audits, Should Lead Vendor Accountability

Episodic vendor audits are better suited for high-risk areas. An oversight system, based on a hierarchy of metrics, provides greater value.

Tech Transfer: 8 Typical Stumbling Blocks To Avoid

Optimize your biopharmaceutical technology transfer by prioritizing clear communication, thorough training, and strategic planning to ensure success.

Rapid Microbiological Methods In Quality Control Of Sterile Drugs

Understand the opportunities and challenges that come with adopting faster, more precise approaches to microbiological testing.

A Biologic Drug's Analytical Journey

Gain valuable insights into advanced methods and analysis techniques for high-order structure, physiochemical characterization, cell-based and biochemical assays, and more.

How To Choose The Right CDMO Partner For Fill And Finish

CDMO selection requires evaluating experience, quality standards, and flexibility. Assess technical transfer skills, supply chain security, and collaborative approach for a reliable, long-term project fit.

De-Risking Development: Characterization Analytics Case Studies

See real-world case studies showing how advanced characterization analytics and mass spectrometry resolve protein quality issues, prevent costly delays, and reduce risk across the lifecycle.

Lessons In Scaling Lipids Production And Purification

The speed at which the pharmaceutical industry is now developing and manufacturing mRNA drug products at large scale is astounding, yet it has highlighted supply chain vulnerabilities in making lipids.

Redefining CAR-T Speed And Strength: A Conversation

Discover how an autologous CAR-T platform is addressing challenges in cell therapy manufacturing. A three-day process shortens cycles, improves T-cell potency and durability, and reduces costs.

Unlocking Efficiency In Large-Scale Microbial Manufacturing

Find out how expert teams and the right tools help build resilience into manufacturing systems and tackle small, often-overlooked issues before they become costly problems.

Accelerating Early Phase Biologics From The Clinic To Commercialization

Strategic planning in early-phase biologics accelerates clinical progress, reduces risk, and lays the groundwork for scalable, compliant manufacturing and successful commercialization.

Transforming Rare Disease Drug Development For A Faster Cure

This comprehensive exploration aims to shed light on the critical aspects of expediting curative therapies, with a focus on the strategic role that CDMOs can play in this transformative journey.

N-1 Perfusion Strategies For Commercial-Ready Biologics

Explore how an approach with modular N-1 perfusion strategies shortens seed train timelines and reduces facility strain, enabling upstream processes that scale efficiently and reliably.

OUTSOURCING SOLUTIONS

Process Characterization CDMO Services - Cytovance Biologics

Advancing Biologic Breakthroughs With Proven Expertise - Samsung Biologics

NanoImprove The Performance Of Your Biologic Formulation - Nanoform

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