Newsletter | September 25, 2025

09.25.25 -- Green Is The New KPI: Sustainability In Pharma Outsourcing

SPONSOR

Explore 20+ new CDMO presenters in quick 20-minute sessions during Outsourced Pharma’s October Partner Week. Sessions include Analytical Services, ADC, Large and Small Molecules, Cell and Gene Therapy, and Fill/Finish. Each session offers a quick, informative look at capabilities to help you find the best-fit partner. Registration, on-demand access, and interactive Q&A are all free.

INDUSTRY INSIGHTS

Navigating Challenges During Formulation Development

Gain valuable knowledge on addressing formulation stability, improving product shelf life, and enhancing overall product performance in biopharmaceutical studies.

Strike The Balance Between Cost-Effective, Risk-Averse Manufacturing

As drug sponsors continue to navigate increasing global demand for complex biologics, it is vital to assess which outsourcing strategies mitigate risk while maintaining budgets and timelines.

Managing Supply For Complex Biotherapeutics

Antibody-drug conjugates' manufacturing supply chain contains five different technologies with specific asset needs: monoclonal antibody, cytotoxic payload, linker, bioconjugation, and fill and finish.

FEATURED EDITORIAL

Green Is The New KPI: Sustainability In Pharma Outsourcing

Sustainability is moving from marketing slogans to precise metering and measurement, as sponsors increasingly look for detailed, facility-level metrics and contract incentives that drive improvement.

Leveraging AI And Data Science For Biologics Characterization

Modern analytical tools produce more data than we know what do with. Artificial intelligence helps condense, interpret, and utilize what's most meaningful.

INDUSTRY INSIGHTS CONTINUED

The Value Of Engaging A Single CDMO For Comprehensive Biologics Services

By forging strategic partnerships with comprehensive CDMOs, see how emerging biopharma firms can navigate through early-phase development and ensure a smooth transition to clinical advancement.

High Viscosity Formulations: Developing A 'Human Solution' To Autoinjector Design

Delivering high viscosity (HV) formulations with a truly human solution involves a balance between safety and practicality. Learn the importance of achieving this solution with HV autoinjector design.

The Strategic Benefits Of Isolator Lines In Manufacturing

Discover how high-speed isolator lines enable sterile, scalable manufacturing for complex biologics and injectables with unmatched efficiency and product integrity.

The Critical Role Of Comparative Analytical Assessments

Utilizing expert analytical testing services can unlock the potential of biosimilars and bring cost-effective treatments to market faster.

Site-Specific Conjugation For Next-Gen ADCs

Unlock the full potential of your ADCs with a site-specific conjugation platform that delivers unmatched stability, homogeneity, and therapeutic performance.

Challenges In ADC Production — Consolidating Operations Under One Roof

Eurofins CDMO Alphora consolidates ADC development and manufacturing under one roof, streamlining processes, enhancing safety, and accelerating delivery of high-quality, clinically-ready ADCs.

SOLUTIONS

Developing A mAb For A Small Biotech Developing Precision Medicines

Corvus, a small biotech developing precision medicines, primarily for oncology patients, was seeking to develop a monoclonal antibody called CPI06, now known as Mupadolimab.

Understand Your Stability Programs

A stability program evaluates how pharmaceutical and biologic products maintain potency, purity, and quality over time, which ensures safety, effectiveness, and regulatory compliance.

Leveraging Advanced Technology And Proven Expertise

By using our proprietary non-viral gene insertion technology, GPEx Lightning ensures rapid development timelines and high-yield production, making it an ideal solution for complex biologics.

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