Insights On Manufacturing Logistics
-
Exploring 4 Patient-Centric Trends Shaping Today's Biopharma Landscape
8/17/2026
Patient centricity is reshaping pharma drug development through supply chain resiliency, decentralized trials, and patient-friendly formulations. Learn what these shifts mean for your pipeline strategy.
-
Efficient Solutions Supporting Freezing And Storage Operations In Bulk Drug Manufacturing
8/13/2026
Practical strategies for reducing handling steps, minimizing product loss risk, and improving operator efficiency in frozen drug substance cold chain operations.
-
De-Risking Automatic Visual Inspection (AVI) Through Integrated Validation
7/30/2026
Aligning visual inspection systems with site standards prevents costly validation failures. Discover strategies to de-risk equipment startup.
-
AST's Latest Generation GENiSYS® R: Available With Accelerated Delivery
7/28/2026
Automated robotic fill-finish and integrated isolator technologies streamline multi-format parenteral manufacturing while ensuring regulatory compliance and maximum yield.
-
Mechanical Engineering Design Process For Combination Products
7/17/2026
Mechanical engineering for combination drug-delivery devices demands more than good design — it requires data-driven risk management from specs through simulation. Learn how a structured phase approach ensures global manufacturing readiness.
-
Considerations In Design And Development Of Novel Combination Drug-Delivery Devices
7/17/2026
Poor scoping kills drug delivery device programs before they start. Learn how to define the right problem, assess risk early, and set boundaries that protect your timeline and budget.
-
Release, Redefined: QC Testing Across In Vivo And Ex Vivo CAR-T
7/13/2026
As CAR-T manufacturing evolves, QC strategies must adapt. Learn how identity, potency, sterility, and safety testing support faster release decisions and broader patient access.
-
Next-Generation Filtration For Enhanced Capacity And Sustainability
7/7/2026
Membrane design has a direct impact on throughput, formulation integrity, and sustainability. See how better filtration decisions can reduce operational bottlenecks and scale-up risk across processes.
-
Optimizing Cold Chain Biomanufacturing Capacity In Brownfield Sites
6/23/2026
Legacy facilities weren't built for today's cold chain complexity. How are CDMOs squeezing more capacity from fixed footprints without breaking what already works?
-
Biologics DP Manufacturing Facility — 1M Vials Per Day
6/15/2026
Our facility features two high-speed vial filling lines capable of producing up to one million vials per day, accommodating fill volumes ranging from 1 mL to 100 mL across a broad range of biologic products.