Newsletter | May 8, 2026

05.08.26 -- STREAM Edition: The Necessity Of Potency Assay Matrices For Complex Proteins

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Digital Ecosystem for Process Intensification

Process intensification can only reach its full potential with a strong digital foundation. Discover how Sartorius digital solutions—combining automation, orchestration, and predictive analytics—enable connected, compliant, and data-driven biomanufacturing. Download the white paper to learn how a unified digital ecosystem supports efficiency and scalability across the entire process chain. Learn more here.

Uncover The Intricacies Of Transposase-Mediated Genome Engineering

Webinar | ATUM

In this presentation, experts provide insight into transposase-mediated genome engineering, genetic quality control, and the maintenance of genetic stability in cell line generation.

Accelerating Your CHO Bulk Harvest Testing Using Rapid Methods

Webinar | MilliporeSigma

With advanced rapid methods that offer both speed and sensitivity, you can expedite your bulk harvest testing and detect adventitious viruses in half the time compared to conventional techniques.

The Necessity Of Potency Assay Matrices For Complex Proteins

Video | Bioprocess Online

For complex proteins, the FDA requires a matrix of orthogonal potency assays. Sponsors must assess all functional activities of a product, especially when the mechanism of action is known.

Aligning Upstream And Downstream Development (Part 1)

Video | Bioprocess Online

In this episode of “Better Biopharma,” panelists from the Bioprocess Online Live event “Optimizing Process Development Through Upstream And Downstream Integration” continue their conversation about how upstream and downstream development teams can work together to accelerate timelines and reduce risks and bottlenecks in process development.

Manual CQV Vs. AI-Powered CQV

Infographic | ValGenesis

Still validating the manual way? With AI-powered CQV, you can reclaim hours lost to protocols and audit prep. What used to take weeks is now done in minutes.

How To Do Quick, Easy Cleanroom Classification

Video | TSI Incorporated

Classification plays a vital role in cleanroom certification and qualification. Discover a particle counter that simplifies testing for adherence to ISO 14644-1, EU GMP Annex 1, or China GMP standards.

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