Newsletter | August 28, 2026

08.28.26 -- For Bispecific Ab Programs, Measure Twice And Outsource Once

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Outsourced Pharma Capabilities Update September 2026: Fill/Finish (Sept 1, 11am ET)

Explore the latest fill/finish capabilities from leading CDMOs, including sterile filling, lyophilization, and advanced packaging. This session highlights available capacity, global facilities, and timelines to support your development and manufacturing needs. Learn how quality control and regulatory compliance ensure product integrity, with concise presentations designed to help biopharma teams connect with partners and make informed outsourcing decisions. Learn more.

INDUSTRY INSIGHTS

Softgel Formulation Strategies For Challenging Oral Compounds

Delve into strategies to solve solubility and permeability challenges, boost oral bioavailability, and ensure consistent absorption — reducing risk and unlocking complex molecules.

Designing Shelf-Stable, Dry Powder Vaccines To Improve Global Access

Spray dry technology is being leveraged to create shelf-stable, dry-powder vaccines to treat and prevent the spread of tuberculosis which could significantly improve our global response to disease.

Innovative Softgel Technologies To Deliver Poorly Soluble Molecules

Learn how to expedite the development pathway for early phase compounds and how lipid based formulations provide an innovative approach to enhance bioavailability for challenging molecules.

FEATURED EDITORIAL

For Bispecific Ab Programs, Measure Twice And Outsource Once

Just like inspecting a house before a major renovation, biopharmas must address underlying bispecific structural and analytical flaws before handing their molecule off to a CDMO.

Unlocking MES Value: Why Technology Isn't The Real Challenge

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

INDUSTRY INSIGHTS CONTINUED

Optimizing Bioavailability With Predictive Science

In silico modeling cut through formulation guesswork for a compound with 0.015 mg/mL solubility, delivering an 8× Cmax and 5× AUC improvement and Phase I progression.

Fast-Tracking FIH To PoC: Strategies For Accelerated Drug Development

Three factors often decide success or failure in FIH studies: integrating biomarkers and pharmacodynamic endpoints, including patients in the trials, and leveraging manufacturing infrastructure.

Choosing A CDMO: 3 Considerations For New Drug Developers

A challenge in drug development can be finding a team capable of carrying a molecule through the complexities between the lab and the patient. See three considerations that build a partnership.

Liquid-Filled Hard Capsules: Applications In Drug Development

Explore the versatility and significance of LFHCs in pharmaceutical and nutraceutical delivery, as well as their role in enhancing drug solubility, bioavailability, and overall efficiency.

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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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