Newsletter | August 24, 2026

08.24.26 -- The U.S. Supply-Chain Uncovered: A Superior Search For Domestic Suppliers

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Outsourced Pharma Capabilities Update: CPHI Milan 2026 Special Edition

The CPHI Milan 2026 OPCU Special Edition is a free virtual event on August 27, 2026, designed for pharma and biotech outsourcing decision-makers. Attendees can preview supplier capabilities, compare CDMOs, CMOs, API, packaging, and service providers, engage in live Q&A, and access on-demand replays. Evaluate partners in advance, prioritize meetings, and maximize your time at CPHI Milan with a focused, informed supplier strategy. Register.

INDUSTRY INSIGHTS

Using Digital Tools In Process Development

Technology can transform the entire biopharma production process chain. Using integrated process models, machine learning, and genetic algorithms has made production faster and more efficient.

Accelerating Biologics With Seamless Technology Transfer

Discover how effective technology transfer strategies can streamline scale-up, maintain product quality, and enable successful clinical and commercial manufacturing.

CDMO Partnerships: Why Speed And Flexibility Matter Now More Than Ever

As demand for GLP-1s and biologics accelerates and timelines compress, it's become more crucial that pharmaceutical companies stay competitive and bring therapies to market by partnering with a CDMO.

FEATURED EDITORIAL

The U.S. Supply-Chain Uncovered: A Superior Search For Domestic Suppliers

The search for supply chain partners goes on. Intensely. But productively? Are we missing anything? We are about to learn the answer to that is yes.  Alan Davis, President & CEO, i5 Services says puzzling is how little these searches vary – and he's concerned that invariance has negative national supply-chain implications. He has a mission and a search platform to change that.

In Bioprocessing, Trusted Data Is A Process Variable

As digital systems become increasingly interconnected, digital validation ensures systems generating and managing GxP data remain accurate, consistent, and trustworthy.

INDUSTRY INSIGHTS CONTINUED

Enriching Sterile Fill/Finish Services With A Patient-Centric Approach

Through early collaboration and advanced aseptic technology, organizations can overcome complex formulation challenges to ensure safe, effective treatments reach patients more efficiently than before.

Designing And Selecting Antibody-Oligonucleotide Conjugates

View antibody-oligonucleotide conjugate design, highlighting antibody formats, linker strategies, and screening methods to optimize delivery, stability, and gene-targeting therapeutic performance.

Mitigating Fill Risk In Drug Product Manufacturing

How robotic, gloveless fill‑finish cuts aseptic risk, enables flexible containers, and scales manufacturing — connecting advanced automation to patient safety and operational efficiency.

Strategic Hiring For Scalable Success

Assimilate how a people-first talent strategy, purpose-driven culture, and cross-functional collaboration come together to support scalable growth and operational excellence in commercial manufacturing.

Increasing Batch Size And Reducing Cycle Times For A Biologic

We partnered with a global pharma company to optimize biologic production, increasing output by 50% and reducing batch release times by up to 30%.

Building Quality By Design For Multi-Specific Therapeutic Proteins

Platforms incorporating high throughput in silico screening, in vitro expression, and immunosafety of multi-specific molecules can help mitigate potential developability risks and accelerate timelines.

The Benefits Of End-To-End Formulation And Fill/Finish Of Biologics

Proper formulation development has a huge impact on whether a technology transfer to clinical phase fill/finish is successful. Review the challenges of transitioning a promising drug candidate.

Three Keys To E&L Success: Study Design, Partner Selection, And Timing

Successful E&L planning starts before testing begins. Aligning study design, partner expertise, and timing helps teams focus on the right risks, avoid surprises, and support stronger development.

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Webinar: Optimizing Peptide Production With PUREcoli™: A Smarter Microbial Approach To Therapeutic Peptide Manufacturing

Therapeutic peptide demand is surging, but traditional synthesis brings cost, scalability, and sustainability challenges. Explore how microbial expression using KBI Biopharma’s PUREplatform™ and PUREcoli™ technology can enable more efficient peptide manufacturing. Using liraglutide as a case study, discover practical strategies to improve yields, reduce costs, and streamline downstream processing for scalable, commercially ready production. Click here to learn more.

SOLUTIONS

Houston, We Have A Complex Biopharma Market!

The Biosimilar Market Reality: Expansion, Risk, And Consolidation

Annex-1 Compliant Robotic Aseptic Powder Fill/Finish Solution

Path To First-In-Human

Recombinant Protein Process Development And Scale-Up

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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