Newsletter | February 10, 2026

02.10.26 -- Putting Pressure On CDMOs With Herman Bozenhardt

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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

Putting Pressure On CDMOs With Herman Bozenhardt

 In this episode of “Better Biopharma,” host Tyler Menichiello is joined by Herman Bozenhardt, a consultant and industry veteran who has spent decades advancing the fields of biopharmaceutical manufacturing, engineering, and regulatory compliance.

Innovation For Subcutaneous Delivery Of Large-Volume Complex Biologics

Explore the key findings of a new wearable injector clinical trial, including its positive impact on patient experience and the broader benefits of wearable injectors for chronic disease management.

Overcoming Barriers To Lentiviral Therapy Commercialization

Review the results obtained for our proprietary HEK293T 2G7 suspension cell line for LVV production by transient transfection in serum-free, chemically-defined and animal component-free media.

How CMOS/CDMOS Drive Industry Growth

From minimizing costs and accessing advanced tech to speeding market entry, dive into how outsourcing drug development and manufacturing to CMOs/CDMOs offers strategic advantages.

Delivering AAV Therapies Via Candidate Screening And Feasibility Studies

As developers begin their AAV therapy research, opting to conduct early phase studies with an experienced CDMO can help mitigate funding challenges and procure material for clinical data.

Scale-Up And BLA Planning For Microbial Biomanufacturing

Early planning for scale-up and biologics license application activities can maximize your chances of success by allowing sufficient time to develop launch options and prevent costly delays and setbacks.

Microbial Biomanufacturing: Where We've Been And Where We Are Going

Learn more about the cutting-edge technologies driving the shift to microbial expression and how the right outsourcing partner can help you leverage the benefits of these innovative therapeutics.

Fast‑Track Pharma Analytics For Resolving Manufacturing Failures

Fast‑Track Pharmaceutical Analytical Services quickly identify and resolve manufacturing failures, reducing delays, controlling costs, and safeguarding patient safety through rapid forensic analysis.

Formulation Through Manufacturing Under One Roof

Partner with a CDMO that understands the unique challenges of emerging biopharma, providing expert guidance in formulation development, manufacturing, and regulatory navigation.

Advancing Drug Product Quality Through AVI And Future-Ready Infrastructure

Automated visual inspection (AVI) combines robotics, precision imaging, and sophisticated defect-recognition software to provide a scalable solution for expanding pipelines.

Optimized ADC Solutions Tailored To The Diverse Needs Of Global Clients

Accelerate the development of next-generation cancer therapies with optimized ADC solutions designed to meet the diverse needs of global clients.

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OUTSOURCING SOLUTIONS

Step Inside One Of America's Leading Protein Biologics CDMO Sites - AGC Biologics

Integrated ADC Offering: From Concept To Commercialization - Lonza

Non‑Animal Pyrogen Detection With MAT - SGS

Production Site Brno (CZ) Clinical/Commercial Syringe Line - medac CDMO

A CMO Delivering Excellence In Every Injection - Pfizer CentreOne

Sterile Drug Product - Curia

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