Newsletter | May 13, 2025

05.13.25 -- The Expanding Role Of CMC In Biotech Investor Decision-Making

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Webinar: Optimizing Biotherapeutic Protein Expression with Novel GS® CHO Vector Technology

Recombinant protein production is evolving to meet growing demand. CHO-based systems remain central, but further innovation is needed. Join us on May 19th to learn how Lonza is enhancing its GS® expression vector technology with a high-strength synthetic promoter to boost yields, maintain quality, and support efficient biomanufacturing across diverse therapeutic proteins. Click here to register.

FOCUS ON OUTSOURCING

The Expanding Role Of CMC In Biotech Investor Decision-Making

With increasingly complex modalities, undruggable targets, rare diseases, and narrowly defined patient subpopulations, CMC is an important area of due diligence scrutiny for prospective investors and licensees. Part 1 of a two-part analysis.

8 Key Partner Quality Attributes Your CDMO Must Have

CDMOs help reduce the complexity and costs of drug development and manufacturing, making the right CDMO partner essential for many biopharma companies.

A New Paradigm In T-Cell Lymphoma Treatment: CD5 CAR-NK

T-cell lymphomas are a complex and increasingly prevalent group of cancers with poor survival outcomes and limited effective treatments, underscoring an urgent need for innovative therapies and novel targets.

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.

Unlocking Potential: A Deep Dive Into AAV Development And Manufacturing

When it comes to furthering AAV's potential in the wider biopharmaceutical pipeline, partnering with a CDMO that can foment an optimal analytical and manufacturing strategy is crucial.

Idea To Clinic: Accelerate Your Manufacturing Timeline To FIH Studies

Translating novel drug discoveries into clinical trials remains a complex endeavor. Learn how a CDMO with cutting-edge technologies can facilitate a smooth path from discovery to FIH studies.

ICP-MS And ICP-OES: Tools For Elemental Impurity Analysis

Leverage advanced elemental impurity testing methods to ensure the safety, compliance, and accuracy of your drug products throughout the manufacturing process.

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Multispecific molecules bring added complexity to downstream purification—think incorrect chain pairings, aggregation, fragmentation, and lower yields. Join Bioprocess Online Live as we explore how developers are addressing these challenges to achieve high purity and efficient processes. Gain insights into key considerations for downstream teams when designing purification strategies for these advanced biologics. Registration is free thanks to the support of Thermo Fisher Scientific.

OUTSOURCING SOLUTIONS

Viral Vectors Made Accessible - VintaBio

Our Biotech Success — Levicept - Lonza

Biologics Discovery, Development, And Manufacturing - Curia

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