Newsletter | October 1, 2026

10.01.26 -- What Makes ADC Tech Transfers So Difficult?

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Antibody Drug Conjugate Manufacturing

Discover how our high-performing equipment, single-use solutions, and expert support can help you design and execute robust, efficient, and flexible ADC operations. Learn more here.

FOCUS ON OUTSOURCING

What Makes ADC Tech Transfers So Difficult?

In this opening segment from the Bioprocess Online Live event “Ensuring Successful Technology Transfer In ADC Development,” panelists Sourav Kundu, Ph.D., and Will Olughu, Ph.D., explain how ADC constructs complicate process and knowledge transfers compared to traditional biologics.

 

 

High Potency APIs And The Evolving Demands Of Drug Development

See how higher API activity is changing expectations around containment, scalability, and cross‑functional alignment — and why early decisions now have a greater impact on long‑term success.

 

The Right Partnerships Are Key To Streamlined Drug Development

Explore how to select the right CDMO partner for your pharmaceutical project to navigate the evolving drug development landscape and ensure successful outcomes.

 

How Sponsors Should Evaluate Manufacturing Resilience

Learn how continuity planning, technology transfer capabilities, global network flexibility, and digital visibility contribute to resilient supply chains and help protect programs from disruption.

 

Flexibility And Capability In Pre-Filled Syringes: The Future Of PFS

Outlined here are the benefits of PFS and how they relate to the delivery of drugs, how SARS-CoV-2 could be fueling an explosive increase in PFS demand, and how a partnership is the key to success.

 

Building A GMP-Ready Cell Line Development Strategy From Day One

Embedding manufacturing and regulatory readiness early streamlines development, reduces delays, and supports successful scale-up.

 

Monoclonal Antibody Lot Release Testing For CHO Cell–Derived Products

Biologic lot testing spans bulk harvest to final stability. Core panels check purity, safety, identity, and potency to ensure compliance, low risk, and high product quality across production.

 

Optimizing Cold Chain Biomanufacturing Capacity In Brownfield Sites

Legacy facilities weren't built for today's cold chain complexity. How are CDMOs squeezing more capacity from fixed footprints without breaking what already works?

 

Where The Future Is Now In Life Sciences And BioPharma

Middlesex County, NJ, is a premier life sciences hub, attracting major biopharma leaders, entrepreneurs, and investors to accelerate global medical innovation.

OUTSOURCING SOLUTIONS

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Capabilities Update July 2026: Gene Therapy - Andelyn Biosciences

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A Digital Platform That Monitors, Predicts, And Controls Bioprocesses - WuXi Biologics

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Advancing Lyophilization Through Formulation, Process Development - Coriolis Pharma

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Delivering LVV Material In An Accelerated Timeline - AGC Biologics

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