This guidance provides the agency’s current thinking on establishing a routine sanitation program for low-moisture, ...

When a pharmaceutical company receives FDA approval for a new therapy, it marks the culmination of years—often over a ...

Tive Solo Pro Tive announced the release of the Solo Pro, a validated, real-time visibility tracker for biologics and ...

BOSTON, April 09, 2025, the global leader in supply chain and logistics visibility technology, today announced the release of the Solo Pro, a validated, real-time visibility tracker for biologics and ...

As oncology research centers scale eSource adoption, the field is shifting toward a fully digital, clinical trial ecosystem.

Discover how Bruker’s BRAVO handheld Raman spectrometer is transforming material analysis with advanced fluorescence suppression and more.

While blood can expire, the verification process before a blood transfusion involves more than just one person, making this ...

PMO governance is a strategic tool for organizations working with the FDA, ensuring projects align with regulatory frameworks ...

The Food and Drug Administration (FDA) announced Thursday it plans to phase out animal testing requirements for biological ...