10.20.26 -- Are You Falling Behind On Intelligent Pharmaceutical Manufacturing?

Developing pediatric and geriatric pharmaceuticals requires strategies beyond tablet crushing, balancing specific age-related palatability and lifecycle management needs for optimal outcomes.

Meeting tight launch timelines requires more than speed. Smart kit design, controlled production workflows, and scalable processes come together to deliver complex packaging programs quickly.

Facility monitoring software with OPC UA client/server functionality makes great business sense. Learn how monitoring leads to reduced waste, improved yield, higher quality, and increased profits.

Particles in medical water systems can cut efficiency and damage components. Layered prefiltration controls contamination, protects equipment, and maintains consistent water quality.

Maximize the oral bioavailability of challenging small-molecule candidates and streamline the path from preclinical toxicology to clinical trials by leveraging optimized lipid-based formulations.

Effective precision weighing systems enable users to balance product throughput, center distance, and standard deviation. Explore key considerations in this technology's development and weighing methods.

Poor manufacturability and immunogenicity can delay development. Gain insight into how early developability assessments support IND readiness.

Discover how medical device companies aim to balance patient safety with environmental stability by offering bio-based UHMWPE, which reduces carbon footprints by up to 70%.

How do we produce recombinant proteins in transgenic fruit flies? Matt Anderson-Baron, Ph.D., provides the deep-dive of a novel biomanufacturing process.

Modeling the human brain requires more than simplified systems. New approaches that incorporate diverse cell types are improving how researchers study neurovascular function with greater precision.

EU GMP Annex 1 now defines clear expectations for glove integrity testing. Examine how reliability, efficiency, and equipment usability are becoming essential factors for maintaining compliance.

Managing challenging active pharmaceutical ingredient crystal structures and choosing dry granulation over wet granulation requires strategic processing choices.

There are two primary filling methods for pre-filled syringes. Delve into the pros and cons of each approach, highlighting why barrel filling is generally preferred in the pharmaceutical industry.

Global expansion and supply chain flexibility are reducing risk and strengthening continuity. See how a multi-site strategy supports quality and customer success worldwide.

Uncover how life science teams build defensible governance, maintain human oversight, and manage regulatory risks when adopting advanced digital tools.