07.15.25 -- Cleaning Process Capability: Understanding Populations, Samples, And Sample Size Requirements

This chapter of The Aqueous Cleaning Handbook explains what an aqueous cleaner is, what it contains, and how it can improve your cleaning process.

In our series on pre-filled syringes, we explore five key ways this delivery format is enhancing patient outcomes, not just through the medicine it contains, but through the device design itself.

Discover five steps to design an EMPQ for sterile manufacturing: classification, protocol drafting, cleaning evaluation, disinfectant efficacy testing, and continuous improvement.

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. Uncover considerations for blender selections.

Pharma leaders face rising pressure to deliver personalized therapies faster and more efficiently. Find out how top companies are evolving operations to stay agile and competitive in a changing landscape.

Learn essential conceptual design principles for transforming alternative spaces into efficient, regulatory-aligned cleanroom environments for your critical processes.

By adopting flow chemistry for a production platform that reduces utility costs and solvent consumption, researchers can overcome the risks and challenges of Butyl Lithium chemistry.

Poor solubility of active pharmaceutical ingredients can hinder drug effectiveness. Read how innovative formulation strategies enhance solubility and bioavailability to improve therapeutic outcomes.

Integrating advanced digitalization solutions and prioritizing data security can accelerate drug development while reducing costs and ensuring consistency across a global network.

Beyond a simple mechanical step, crimping is a critical control point. We examine how advanced rotary technology provides superior seal quality, particulate control, and data-driven compliance assurance.

Product design, production methods, and supply chain can be leveraged to positively impact sustainability through effective planning.

Validation in GxP environments is often the bottleneck in digital transformation—manual, repetitive, and complex. One company's Intelligent Agents are transforming that process.

Gain insight into key strategies and technologies designed to address the analytical considerations and material flows to facilitate the rapid delivery of toxicological material.

Explore how Germfree designed and installed a mobile cGMP cleanroom on a 53′ tractor-trailer chassis to provide a flexible and efficient cleanroom solution tailored to the company’s needs.