04.05.24 -- Navigating Grades And Sources Of Materials In Drug Manufacturing

Learn about monitoring viable and non-viable particles during the fill/finish process of drug manufacturing as well as considerations for the location of airborne particle monitors.

Read about the identification of CMAs, CPPs, and CQAs of drug products and how to predict their impact on formulation and manufacturing processes.

A systematic approach determines the best disinfectant solution for a facility. Examine the variables that impact disinfection of surfaces, including tool selection and the application of disinfectant solutions.

Explore the importance of isolators in the pharmaceutical and biotech industries, the challenges of innovating aseptic isolator design, best practices, and key aspects of design optimization.

How do you know if an intensification approach will provide advantages? Three process intensification experts show how various intensification approaches affect outputs using different scenarios.

What are the benefits of using automated product data management and quality management system software solutions in manufacturing?

Aside from the level of shear or ‘gentleness,’ a number of other factors help determine which type of blender will work best in certain applications. Explore considerations for blender selections.

In today's fast-paced global economy, maintaining data quality in chromatography analysis is more difficult than ever before. Discover how you can achieve complete confidence in your QC lab data.

Learn about an offering designed to simplify and accelerate the development pathway, even for APIs with challenging properties, such as low aqueous solubility and poor bioavailability.

Explore a single-use chromatography system that introduces micro-efficiencies into the manufacturing workflow process, potentially leading to time and cost savings throughout the production life cycle.