Newsletter | February 24, 2026

02.24.26 -- January 2026 — CDMO Opportunities And Threats Report

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FOCUS ON OUTSOURCING

January 2026 — CDMO Opportunities And Threats Report

Each month, Outsourced Pharma works in conjunction with PharmSource, part of GlobalData, to present its “Contract Manufacturing: Opportunities and Threats (CMOT) Report” to our readers. The report identifies CDMOs that might be impacted by key events affecting their clients, including company acquisitions, product acquisitions and licenses, product approvals, late clinical product terminations, and FDA rejections.

A Guide To Analytical Characterization Of Complex Molecular Formats

A thorough and adaptable analytical strategy is essential for navigating the complex mAb market. This approach boosts the likelihood of market approval and unlocks the full potential of these therapies.

Enabling Digital Twins With Computational Fluid Dynamics Modeling

Embrace the transformative power of predictive modeling and digital twin technology to optimize bioprocess efficiency, ensure product quality, and drive innovation in biopharmaceutical manufacturing.

Seamless Onshoring From China-Based CDMO

Successfully mitigate geopolitical risk and maintain supply continuity. Learn how a large-scale manufacturing process was rapidly requalified in eight months to secure a clinical-stage biologic program.

Advancing Scalable Vector Production For AAV-Based Treatments

Enable scalable, high-yield AAV manufacturing with minimal contamination that delivers >10¹⁷ genome copies per 200L run and supports efficient, GMP-compliant production for diverse serotypes.

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

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

Analytics And Bioassays Can Safely Fast-Track mRNA-LNP Development

One main mRNA technology challenge is the formulation of delivery systems like LNPs. Learn about evading impurities in lipids, the future of mRNA-based genomic medicines, and more.

Sterile Filling Readiness In The Drug Device Delivery Ecosystem

Explore how adaptable technologies and strategic partnerships help navigate Annex 1 compliance and technical hurdles to ensure the successful delivery of complex drug products.

Analytical Considerations For mRNA-Based Therapies

Uncover why leveraging strong scientific expertise and comprehensive testing techniques will be vital in expediting development and upholding the integrity of these life-saving treatments.

How Integrated Data Systems Enhance Clinical Development

Delve into how cloud-based systems and unified data platforms are transforming biomanufacturing by enhancing efficiency, ensuring quality, and accelerating the delivery of complex therapies to market.

Minimizing Risk In RNA-LNP Encapsulation And Drug Product Manufacturing

Gain insight into an integrated drug substance/drug product offering for your IND program and beyond, with a holistic approach to ensure process robustness at every stage.

Beyond Geographies — Derisking Global Manufacturing

Discover how to mitigate risks in global pharmaceutical manufacturing by learning from Joon Chang and Tracey Partington’s decades of industry experience.

Sustainability Report

Operational excellence meets ethical stewardship. Data-driven strategies and renewable energy integration are shaping a responsible future for global manufacturing and community engagement.

OUTSOURCING SOLUTIONS

Path To IND For Biologics Delivers Phase 1 Material In 9 Months - Thermo Fisher Scientific

mRNA/LNP Development And Manufacturing Services - Lonza

Viral Clearance Testing For Biologics, Vaccines, And AAV - Minaris Advanced Therapies

iPSC Differentiated Cell Products - Applied StemCell

User-Friendly Disposable Autoinjector - BD Medical - Pharmaceutical Systems

Sterile Injectable End-To-End CDMO Services - August Bioservices

You Make The Discovery. We Help Make It Reality. - Avid Bioservices

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