03.10.26 -- U.S. Pharma Tariffs And MFN In 2026: Manufacturing And Procurement Impact

Aseptic blow-fill-seal systems for packaging pharmaceutical liquids incorporate materials and processes that provide critical advantages for sustainable initiatives.

Relying on fragmented data becomes problematic when teams need to dissect cell line performance data and that data is not in a digital backbone.

Improving pediatric adherence requires age-appropriate formulations, taste-masking, and swallowability strategies. Regulatory and technological insights help overcome barriers and support safer therapies.

In the CCIT space, one single inspection technology cannot be used for every type of pharmaceutical product. You should always weigh the various factors to determine the ideal inspection methodology.

Explore the formulation and manufacturing of a topotecan inhaled dry powder and its use in decreasing tumor size in an animal model.

See how Agentic AI sharpens batch release workflows by surfacing faster insights, reducing manual effort, and giving teams clearer oversight. It offers a more organized, collaborative, and compliant route.

A practical USP <1665> and <665> framework helps manufacturers evaluate and manage extractables and leachables risk, supporting quality, safety, and regulatory compliance.

Learn why generic EAM systems fall short in regulated industries and how purpose-built solutions ensure compliance, efficiency, and audit readiness.

Transferring visual inspection data from paper to digital is essential for Pharma 4.0 compliance. Discover practical strategies to eliminate errors, automate data tracking, and enhance quality assurance.

Ensure personnel safety during hazardous material handling by mastering airflow dynamics. Gain insight into how to achieve low exposure levels through advanced HEPA filtration methods.

Streamline mAb purification with confidence. Examine practical considerations for developing processes with advanced mixed-mode chromatography, ensuring superior impurity and viral clearance.

The pre-filled syringe space is one of the fastest growing pharma sectors, offering greater patient safety and lower manufacturing costs. But pre-filled doesn’t translate to easily filled.

A new algorithm developed by a real-time viable particle counter determines the viability of a particle based on its measured optical properties, improving the detection of microorganisms.