Newsletter | February 5, 2026

02.05.26 -- Building Enterprise Resilience From QRM Signals

SPONSOR

Join Bioprocess Online Chief Editor Tyler Menichiello on February 11, at 11 a.m. Eastern, for an interactive panel discussion exploring how upstream and downstream development teams can work together to reduce risk, accelerate process scaling, and support smoother downstream tech transfer. Register for free thanks to support from Ecolab.

FOCUS ON OUTSOURCING

Building Enterprise Resilience From QRM Signals

Turn enterprise resource management (ERM) from a checklist into a true decision system — so risk informs everyday choices before quality events become supply disruptions, delays, or regulatory exposure.

The Value Of Engaging A Single CDMO For Comprehensive Biologics Services

By forging strategic partnerships with comprehensive CDMOs, see how emerging biopharma firms can navigate through early-phase development and ensure a smooth transition to clinical advancement.

BsAb Development With Structural Innovation, Enhanced Manufacturability

Bispecific antibodies (bsAbs) offer transformative therapeutic potential through dual-target engagement, but their complex structure presents significant manufacturing challenges.

Progressing A Cystic Fibrosis Treatment With A Strong Culture Match

Collaborate with an experienced CMO that combines transparency, expertise, and a shared commitment to help advance complex biologics from preclinical research to clinical success.

Accelerate And De-Risk Bioconjugate Drug Development

With a growing interest in developing new and improved bioconjugate drugs, explore an “innovation through collaboration” approach that can facilitate access to next-generation conjugation technologies.

Quadrupling Inspection Speed With Automated Visual Inspection (AVI)

Examine how vaccine vial inspection can be boosted with automated visual inspection to improve accuracy, efficiency, and capacity to 20 million vials annually.

How To Develop Reliable, Repeatable Microbial Processes At Any Scale

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

In Vivo RNA Tuning for Liver Gene Editing Efficiency

RNA sequence and guide modifications, delivery platform design, and dose optimization all contribute to improved gene editing outcomes, which offer a clearer path toward scalable mRNA-based therapeutics.

Why Use Transposase Technology For Expression Of Your Biotherapeutics?

Discover how a proprietary transposase technology works and why it can be beneficial for the development process for the expression of biologics.

Transitioning From Clinical Phases To Commercial Readiness

CDMOs must have unique abilities to complete your project within your timeline. Gain insights as an industry expert reviews one of the most sought-after and fastest-growing CDMOs in the industry.

Successfully Producing Insoluble Proteins Using Inclusion Bodies

Review the pros and cons of soluble and insoluble processes, experiences with isolating, solubilizing, and properly re-folding, and strategies and innovation to improve insoluble processes.

OUTSOURCING SOLUTIONS

Advanced CHO Cell Line Development For High-Yield Biologics - KBI Biopharma

Quality Control Services - Argonaut Manufacturing Services

Access To Medicine In A Way The Industry Hasn't Seen Before - FUJIFILM Biotechnologies

LEG14-Mediated TCR Knock-In For T-Cell Engineering - ElevateBio

State-Of-The-Art CDMO Facility - Maple Grove - Bora Pharmaceuticals

Tailored CDMO Solutions With Unmatched Quality - LOTTE Biologics

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