Newsletter | April 10, 2025

04.10.25 -- Questions You And Your New CDMO Might Be Asking

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The debate rages on. While the automation that enables continuous processing gets a lot of hype, there are plenty of dyed-in-the-wool biopharma pros who contend that process optimization and intensification yield comparable benefits, without requiring the capital-intensive process overhaul that continuous demands. Join Bioprocess Online Live for a virtual deep dive into the scalability, sustainability, and capital implications of the continuous-versus-optimized debate. Registration is free thanks to the support of Cytiva.

FOCUS ON OUTSOURCING

Questions You And Your New CDMO Might Be Asking

One expert who has been on both sides of contracting relationships explores common questions you could — or should — be asking before signing up with a new manufacturer.

5 Biologics Conferences You Won't Want To Miss In 2025

Mark your calendar for these five pivotal biologics conferences in 2025, offering a unique blend of scientific insights, networking, and glimpses into the future of biotherapeutics.

Tackling Cell & Gene Therapy Manufacturing Challenges

Allogeneic therapies are gaining popularity due to diversity, scalability, and affordability. A partner with innovative solutions can help streamline the path from discovery to commercialization.

Mitigating Oxygen Heterogeneity In Large-Scale Bioreactors

Oxygen heterogeneity, caused by pressure variations and other factors in large-scale bioreactors, can significantly impact cell growth and product yield.

Driving Operational Excellence Using Machine Learning

Explore how advanced machine learning and data analytics are revolutionizing biopharmaceutical manufacturing and driving operational excellence.

Enabling CDMOs To Focus On Core Priorities

Discover solutions that help CDMOs meet the challenges of the recent CDMO market segment growth in biopharmaceuticals, including partnership with reliable cGMP chemical suppliers.

The Right Scale At The Right Time To Accelerate Your Market Supply

Learn about the challenges in today’s changing market and solutions to help successfully develop and manufacture lifesaving products.

The Benefits Of Streamlining And Standardizing Plasmid DNA

The need for greater volumes of high-quality raw materials like plasmid DNA in the cell and gene therapy space has made pDNA standardization integral to streamlining the development process.

OUTSOURCING SOLUTIONS

Capacity Update January 2025: Large Molecule Development - Cytovance Biologics

Capacity Update January 2025: Large Molecule Development - KBI Biopharma

Capacity Update January 2025: Large Molecule Development - Northway Biotech

Unraveling ADC Complexities With Bio-Logic Brilliance - Pfizer CentreOne

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