05.15.25 -- AI Model Cards Make Function And Risk Easier To Understand

Oral GLP-1 formulations represent a groundbreaking advance in obesity treatment to offer improved patient comfort and adherence while expanding the therapeutic market.

Discover how strategic partnerships, robust process development, and a keen awareness of supply chain vulnerabilities can pave the way to a successful clinical trial.

CAPA management is vital for quality systems, especially in pharmaceuticals. Examine how issues are identified, corrected, and prevented to safeguard health and uphold regulatory compliance.

Review the role of solid form screening and PBPK modeling to enable accelerated timelines desirable in early-phase drug development. Explore formulation maps for ASDs and key criteria for salt screening.

Uncover how to enhance your pharmaceutical production efficiency with an intelligent MBR design that offers tailored software, handling systems, and inspection machines.

Reveal the processes and technologies being utilized by life sciences manufacturers to achieve success on their Industrial DataOps maturity journey, as well as real-world best practices from the field.

Freeze-drying stabilizes biologics but requires optimizing parameters like temperature and structure. Learn how modulated DSC™ improves precision in analyzing transitions.

Find out why it is critical that OEMs see and understand the benefits of taking time to build a mold or create automation more robustly to achieve long-term savings and higher annual production.

See why high-performing filters are inadequate for critical filtration processes and why sterilizing-grade filters are necessary to effectively remove undesirable species, including bacteria and viruses.

To accelerate COVID-19 vaccine production, a leading biologics contract manufacturer sought high-speed labeling machines that could be rapidly deployed.

Read more to investigate how particle size, morphology, and deposition profiles are affected by the scale-up of the spray drying process.