Newsletter | May 20, 2026

05.20.26 -- Kodak's CEO Leans Into Pharmaceutical Manufacturing – "I'm An Operator"

INDUSTRY INSIGHTS

Strategy, Innovation And The Future Of CDMOs

Explore expert insights on the forces reshaping the CDMO landscape — from onshoring and capacity investment to patient-focused innovation — and what it takes to stay at the forefront.

Your Guide To Minimizing Scope Creep For Pharma Projects

By adopting these best practices, biotech sponsors can foster more transparent, efficient, and productive collaborations with their CDMO partners.

De-Risking Early Phase Micronization With Integrated Solid Form Selection

Review the crucial selection of the optimal solid form in  carefully achieving successful jet milling of APIs designed specifically for pulmonary administration through the pulmonary route.

FEATURED EDITORIAL

Kodak's CEO Leans Into Pharmaceutical Manufacturing – "I'm An Operator"

Kodak – the company and Eastman Business Park in Rochester, NY. – was the focus of a recent editorial. But the man in front of Kodak’s attempted comeback is Jim Continenza, Chairman and CEO, is a topic unto himself. He is as animated as any public-company CEO you’ll encounter. And he knows his audience; early in his conversation with Chief Editor Louis Garguilo he says Kodak has always supplied CDMOs and the industry with important chemicals. Today he brings the industry an animated articulation of manufacturing suppliers.

Why Isolators Do Not Automatically Ensure Annex 1 Compliance

Isolators are powerful tools, but they do not automatically ensure compliance with EU GMP Annex 1. RABS are frequently dismissed too quickly. The difference is not the technology itself, but how it is applied.

INDUSTRY INSIGHTS CONTINUED

IP Considerations In Drug Development For Biotech Companies

Integrate a strategic intellectual property approach early in drug development to streamline research, uncover opportunities, and maximize the return on your investment.

Approach To Improve Solubility And Bioavailability: Spray Drying

Accelerate your drug development by leveraging spray drying expertise to identify optimal drug–polymer combinations that enhance stability, solubility, and in vivo performance of amorphous formulations.

Decoding ADC ADME With Tailored Strategies

Overcome the complex ADME and DDI challenges of antibody–drug conjugates with tailored, data-driven strategies that accelerate development and support regulatory success.

Re-Thinking ASD Development: When Your Molecule Breaks The Rules

A solvent‑free, fusion‑based approach streamlines amorphous solid dispersion development, enabling rapid early screening, improved performance, and sustainable manufacturing.

SOLUTIONS

Time-To-Manufacture Reduced By 30% Through Rapid Transfer Strategy

Commercially Proven Sterile Fill/Finish With Capacity And Global Backing

Your Integrated Drug Substance Partner

Oral Solid Dosage Development And Manufacturing

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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