Newsletter | February 4, 2026

02.04.26 -- At JP Morgan 2026, Few Showed Up For U.S. Manufacturing

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Join Outsourced Pharma Chief Editor Jeff Buguliskis and our panel of industry experts as they share practical advice, reveal what to look for beyond the surface, and answer your toughest questions about selecting a CDMO partner that can truly deliver. Register for free today!

INDUSTRY INSIGHTS

How To Achieve Smarter, Scalable Flow Chemistry

Designed for scientists and engineers evaluating advanced reactors, this recording delivers practical insights and real-world examples to support safer, more efficient, and adaptable flow chemistry.

Building A Resilient Supply Chain For Your Next-Generation Peptide Therapeutic

As peptide therapeutics continue to establish themselves as a leading technology for treating chronic indications, drug sponsors must identify peptide building block suppliers to secure starting materials.

Considerations When Outsourcing Your Packaging Operations

Explore the key to maintaining and enhancing existing and new partnerships as well as how outsourcing one crucial aspect of bringing products to market can benefit overall supply chain optimization.

FEATURED EDITORIAL

At JP Morgan 2026, Few Showed Up For U.S. Manufacturing

What may turn out to be an instructive anomaly emerged at the JP Morgan Healthcare Conference. Across eight roundtable discussions convened by biopharma investment advisors Treehill Partners – covering topics such as Avoidable Drug Development Pitfalls and The Emergence of Highly Competitive Chinese and Korean Biotech – the one session where nary a soul showed up was titled: U.S. Manufacturing. “I don’t quite understand it,” says Ali Pashazadeh, Treehill founder. Here's an investigation.

The 5-Layer Fix For AI Failure In Pharmaceutical Manufacturing

The promise of AI is colliding with the harsh reality of data chaos in pharma manufacturing. This article explores why most AI investments fail, and a 5-layer solution.

INDUSTRY INSIGHTS CONTINUED

"Ultra High” Potency Development And Manufacture

A biotech with limited experience in the development and manufacture of high potency compounds sought to develop a process for producing a highly potent API used to treat an unmet oncology need.

Less Mess, Less Stress, Best Expressed: An Alternative To Spray Drying

Although well-established processes, spray drying and hot-melt extrusion can be outperformed in bioavailability, cost-savings, manufacturing speed, environmental impact, and more.

Pharmaceutical Spray Drying: Sustainable Commercial Best Practices

Learn more about defining the spray drying process with an emphasis on specific enhancements to accommodate scale-up to commercial scale equipment of challenging applications or molecules.

Use Of Reconstructed Tissue And 3D Printed CT-Based Nasal Casts

Reconstructed nasal epithelium and CT-based 3D nasal casts provide more predictive, physiologically relevant models for assessing nasal drug delivery, improving accuracy in formulation development.

SOLUTIONS

Expert Formulation, Reliable Results

Choose an experienced CDMO specializing in high-potency softgels and liquids to ensure high-quality products, responsive service, and reliable solutions across complex therapeutic areas.

Small Molecule Drug Product/Finished Dosage Form

Dr. Rebecca Coutts highlights PCI’s high potent oral solid dose (OSD) and oral liquid capabilities, focusing on site expertise, specialized infrastructure, and handling of complex molecules.

A New Era Of High-Performance Fill-Finish

See how modern filling infrastructure is driving efficiency, enhancing flexibility, and supporting long-term expansion within the injectable manufacturing space.

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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