Newsletter | September 22, 2026

09.22.26 -- Using Digital Platforms To Find Your CDMO

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Webinar: IND in as Little as 6 Months: Now Beyond mAbs

Accelerating biologics development doesn’t have to mean compromising quality or scalability. Join Lonza to explore expanded DNA-to-IND pathways for mAbs, bispecifics, Fc-fusions and high-concentration biologics. Through data, case studies and practical insights, discover how expression technologies, integrated CMC strategies and streamlined execution can reduce timelines, support IND readiness and enable efficient development from early stages through future milestones. Click here to learn more.

FOCUS ON OUTSOURCING

Using Digital Platforms To Find Your CDMO

In recent years, digital platforms have emerged to help pharma/biotech companies discover, evaluate, and connect with CDMOs more efficiently. These resources have different functions and limitations.

 

 

Building Late-Stage Efficiency Into Biologics Development

Building late-stage efficiency early in biologics development prevents scale-up delays. Flexible platforms and risk-based validation streamline technology transfer and lower production costs.

 

Navigating Complex OSD Challenges With Predictive Insights

Learn how predictive modeling, advanced material characterization, and data-driven process insights support manufacturing readiness and confident launch decisions.

 

A Launchpad For Life Sciences Startups And Entrepreneurs

Middlesex County, NJ, is a hotbed for the life sciences, offering a deep talent pool, an extensive R&D presence, and dedicated backing by local government in the form of strategic investment.

 

When High-Stakes ADC Decisions Can't Wait For More Material Or Better Data

Learn how a material-sparing analytical workflow can generate reliable data, reduce dependence on calibration assays, and support faster, more confident candidate evaluation.

 

6 Trends Redefining Biologics Manufacturing In 2026

Biologics manufacturing is evolving through smarter fill technologies, onshoring, advanced automation, and data driven processes that improve efficiency, reduce risk, and protect product value.

 

How To Develop Reliable, Repeatable Microbial Processes At Any Scale

Developing scalable microbial fermentation depends on optimizing growth and expression phases through efficient oxygen transfer, fine-tuning of nutrient delivery, and induction of protein expression.

 

Setting A New Benchmark For Sustainability In Contract Manufacturing

Operational excellence meets ethical stewardship. Data-driven strategies and renewable energy integration are shaping a responsible future for global manufacturing and community engagement.

 

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.

OUTSOURCING SOLUTIONS

A New Player With A Long History - Andelyn Biosciences

Sterile Drug Product - Curia

From Cell Line To Clinic: 4 Months Sooner With mAb Accelerator - Syngene International Ltd.

Don't Just Launch Your Molecule, Protect It! - West Pharmaceutical Services, Inc.

pDNA Manufacturing - 53Biologics

From Sequence To Clinic: Faster Decisions Through In Silico Insights - Coriolis Pharma

Optimizing CGT With Lean Principles - ElevateBio

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