Newsletter | September 9, 2026

09.09.26 -- Don't Fear The Machine – A Biologist Explains AI In The BioPharma Industry

SPONSOR

 

Webinar: Accelerating To The Clinic: Building Oral Dosage Forms For Speed Today And Success Tomorrow

Moving oral solid dosage forms into the clinic quickly requires more than speed. It requires a structured approach that supports flexibility, decision-making, and long-term success. Join Bend Bioscience to explore how biopharmaceutics modeling, formulation, analytical, manufacturing, and quality strategies can accelerate Phase I readiness, reduce rework, and build a stronger foundation for later-stage development. Click here to learn more.

INDUSTRY INSIGHTS

 

Overcoming Product Instability And Improving Yield

Early identification of hidden product instability enabled rapid process adjustments, improving yield and keeping a preclinical toxicology program on track despite challenging reaction conditions.

 

Integrating Molecular Design And Enabling Formulation

Explore how integrated molecular design and formulation strategies can overcome the unique oral-delivery challenges of PROTACs, transforming complex degraders into viable, scalable medicines.

 

Spray-Dried Dispersions Enable Local Delivery For Lung Cancer

Learn more about spray drying, and explore case studies detailing its success as a critical tool in developing innovative and effective lung cancer therapies.

FEATURED EDITORIAL

Don't Fear The Machine – A Biologist Explains AI In The BioPharma Industry

"I should have known," writes Chief Editor Louis Garguilo, "It takes an accomplished biologist to most effectively describe the significance of artificial intelligence in our outsourcing industry and how to put it to practical use." That professional is Damiano Dragone, Founder & Principal Advisor, Dragone Consulting, who built a career across pharmaceutical quality and data-driven quality environments within the biopharmaceutical industry, and was an early proponent of the promise of AI in development and manufacturing processes and facilities.

 

Turning Your eQMS Into A Strategic Quality Advantage

This article addresses everything that follows the signed contract for an eQMS: how a system is configured, validated, adopted, and maintained.

INDUSTRY INSIGHTS CONTINUED

 

Secondary Packaging: Labeling, Cartoning, Clamshell, And Stretch Carding

Tight timelines and coordinated packaging execution drove a high-stakes product launch ahead of a national competitor, ultimately capturing over half the market and setting a new benchmark.

 

Sterile Filtration Following Aseptic Processing

When terminal sterilization isn't an option for heat- or radiation-sensitive APIs, sterile filtration with aseptic processing protects quality. Get the technical framework.

 

Accelerating Development And Enhancing Pipeline Value

Discover 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 streamlined partner.

 

Balancing Speed And Compliance In Oral Dosage Development

This paper highlights how the roller compaction process not only enhances efficiency but also improves the scalability of solid oral dosage production, supporting rapid development for regulatory approval.

SOLUTIONS

Nanomilling: Enhancing Drug Solubility And Bioavailability

Supporting Small Molecule Growth From Clinic To Commercial

Advancing Nitrosamine Testing For Evolving Regulations

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.

 

Connect With Outsourced Pharma: