Newsletter | June 12, 2026

06.12.26 -- Data Confirms Europe's CDMOs Succeed Despite U.S. Gyrations

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Outsourced Pharma Capabilities Update - ADCs

This digital event focuses on antibody-drug conjugates (ADCs) and how CDMOs support their development from early stages through clinical and commercial manufacturing. It highlights the importance of selecting the right partner for these complex therapies, including expertise in conjugation processes, scalability, regulatory needs, and integrated development services. Attendees will learn key criteria for evaluating CDMOs and how to align partnerships to accelerate ADC program success. Click here to learn more.

INDUSTRY INSIGHTS

Redefining Prefillable Syringe System

This step-by-step flow helps guide teams from early feasibility assessments all the way through to regulatory submission, with greater clarity at each stage.

An Industry Approach To Adsorb Lipids Onto Powder Substrates

Explore innovative solutions for improving the solubility and bioavailability of poorly soluble compounds in solid oral dosage forms to enhance drug delivery and therapeutic effectiveness.

Dry Powder Inhalable Vaccines For Shelf Stability And Global Access

What if a formulation that removed the need for cold chain distribution was possible? Examine the formulation of vaccines and manufacturing considerations for dry powder inhaled vaccines.

FEATURED EDITORIAL

Data Confirms Europe's CDMOs Succeed Despite U.S. Gyrations

Confirming data is now at hand. In 2005, we suggested Europe’s CDMOs couldn’t wait for a political or trade détente vis-à-vis the U.S. If they actively leveraged their reputation for reliability, tariffs would not meaningfully redirect manufacturing to the U.S. Here's an analysis of a GlobalData report on what has transpired.

The Future Of Continuous Is Integrated Manufacturing: The 4 Misconceptions About A Lean Process

Pharmaceutical continuous manufacturing is an enabler of better manufacturing, but only when implemented with intention.

INDUSTRY INSIGHTS CONTINUED

Gaining A Competitive Edge Through Regulatory Compliance Confidence

Achieving regulatory compliance confidence is paramount for safety and competitive advantage. Adherence to standards and robust risk mitigation are essential to avoid delays.

Safely Scaling High Potency API Manufacturing

Scaling HPAPI production demands disciplined containment and exposure control. Integrated operating models help manage risk while enabling compliant, reliable scale‑up.

Why Early Formulation Decisions Matter

Rushed OSD formulation decisions create costly downstream failures. Learn how strategic early-phase planning reduces CMC holds, scale-up risks, and regulatory delays.

Enhancing Drug Performance Through Lipid-Based Formulations

Advance CNS-penetrant therapies by optimizing oral formulations to improve bioavailability, stabilize the API, and deliver more consistent and reliable drug exposure.

SOLUTIONS

Advanced Aseptic Filling Line: Vials, Syringes, And Cartridges

Accelerate NCE Discovery With India-Based Medicinal Chemistry Expertise

Testosterone API Catalog

OUTSOURCED PHARMA CAPABILITIES UPDATE

Find Your New CDMO At Outsourced Pharma Capabilities Update

CDMOs in biologics, cell and gene, and small molecule share their capabilities and available capabilities. See for yourself why this virtual event has become a wildly popular resource to identify options for your development and manufacturing needs.

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