Newsletter | May 27, 2026

05.27.26 -- Why Is Biopharma Left Out Of The U.S. Infrastructure Conversation?

INDUSTRY INSIGHTS

Advancing High Potency Manufacturing

Advance potent drug manufacturing through tighter containment, thoughtful process engineering, and closed handling that protects workers while improving efficiency and scale.

Minitablets: Enhancing Safety And Palatability For Pediatric Medicines

Leverage minitablet technology to create flexible, easy-to-swallow, and palatable pediatric formulations that improve adherence and meet evolving regulatory requirements.

Enhancing Micronization Processes With Mesoporous Silica

Discover how using mesoporous silica as a means to enhance the micronization process is redefining the path to more efficient and reliable API formulation.

FEATURED EDITORIAL

Why Is Biopharma Left Out Of The U.S. Infrastructure Conversation?

Gigantic investment manager BlackRock recently gathered powerful investors to discuss along with government officials the nation’s physical and economic backbone. The conversation targeting infrastructure was expansive, but from our vantage point, incomplete. During the 2026 BlackRock Infrastructure Summit discussion of biopharma needs was conspicuous by its absence. How can that be? What industry is more important and more reliant on infrastructure of all kinds? Analysis from Chief Editor Louis Garguilo.

Closing The MES Value Gap: Why Technology Isn't The Problem

Manufacturing execution system (MES) technical maturity is rising, but adoption across manufacturing sites is uneven. Organizational readiness may hold the key.

INDUSTRY INSIGHTS CONTINUED

Navigating Complexity: Tailored Analytical & Preclinical Services

Analytical and preclinical strategies identify risk early, integrate data-driven insight, and streamline formulation planning to accelerate timelines and position molecules for successful development.

Human Skin Explant Model For The Investigation Of Topical Therapeutics

Learn more about an ex vivo cultured human skin explant model in which pathological tissue integrity, barrier function, and metabolic stability have been characterized over time.

Overcoming API Constraints And Tight Timelines

Use innovative lipid-based formulations and on-demand manufacturing to accelerate Phase 1 trials, enable flexible dose escalation, and maximize limited API for poorly soluble compounds.

How Our Drug Development Model Enhances eNPV

See how an integrated CDMO and CRO model can accelerate development timelines, add up to $62.9 million in value, and help you maximize long-term pipeline success with a single partner.

SOLUTIONS

Hydrocortisone API Catalogue

Advancing Drug Development With AI-Enabled Synthesis Approaches

Regulatory Starting Materials (RSMs) — India

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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