The new cleanroom at our global headquarters in Salt Lake City, Utah, was designed for today's rigorous contamination control expectations, driven by EU GMP Annex 1. Learn More
Blog Post 11 – Crystals in Bloom: Unraveling the Solubility Puzzle 2 min reading time Followers of our blog series will notice that a routine ultraviolet (UV) liquid chromatography (LC) analysis is often the first step in detecting that something...
Blog Post 2 – MIND THE LABEL: rapid impurity identification through in-house intelligence 2 min reading time Even subtle changes in secondary packaging can introduce unexpected impurities into drug products—posing risks to quality and patient safety. In this first case...
In this article Jennifer Gygi, Expert Technical Consultant at Nelson Labs, discusses how EO-optimization efforts can affect a manufacturer’s packaging validation. Read the Full Story in MPO
Large-volume parenteral (LVP) applications are characterized by high-volume doses of a drug product, which are administered intravenously. Flexible-bag systems, which contain a combination of different materials, are often used as container or closure systems. First in this webinar, definitions and...
Within our industry, we have seen several approaches to selecting samples sizes, this paper will not cover all of the approaches, but it is a guide to give medical device manufacturers and pharmaceutical companies a good starting point for determining...
