02.28.25 -- Comparison Of Sterilization Methods: Vaporized Vs. Aerosolized Hydrogen Peroxide

To guide a biotech through successful drug development, there are three key areas a CDMO should focus on: equipment and instrumentation, organization and personnel, and systems and processes.

Watch expert Kathianne Ross explore ALCOA+ principles, audit preparation strategies, and the role of digital validation in enhancing compliance and audit success.

Several key factors influence the choice of CCIT technology. Explore how methods like high voltage leak detection, headspace analysis, and vacuum and pressure decay can help when applied.

With so many different media available that vary widely in properties and composition, it is important to know how to select a dissolution media that can effectively test formulation robustness.

Examine why Medtech OEMs, contract manufacturers, and other partners involved in the device life cycle are increasingly realizing additional benefits by making sustainability a group exercise.

Learn how a recent project applied process improvement methodology to the process validation step that ultimately provided not only an optimized, robust process but also an economic advantage.

Discover the potential of a modular operations platform that scales the benefits of digitalization and aids organizations in implementing a unified data strategy to realize the full potential of smart manufacturing.

Gain insight into how technology is helping Recipharm in Pianezza reduce aluminum foil consumption in blister production by 30 percent while maximizing efficiency.

In an industry where unplanned downtime during manufacturing can be catastrophic, having the right maintenance support for the highly specialized equipment supporting a biopharma workflow is crucial.

The delivery of this mobile cGMP cleanroom facility to ACT showcases Germfree’s commitment to providing innovative solutions that meet clients' unique needs and contribute to advancing healthcare.

Failure to identify a compound’s red flags early in development often manifests as program delays or failures. Find out how to avoid these setbacks through complete molecular characterization.

Environmental considerations in pharmaceutical manufacturing strategies have become increasingly important in the face of additional calls to address pollution and sustainability practices globally.

Explore the advantages of a filling technology that provides faster readiness to good manufacturing practices (GMP) filling compared with traditional options.

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