Adding steps to traditional method validation delivers higher ROI.

Crystallization is the most common method used for final purification and isolation of the active pharmaceutical ingredient, or API, when synthesizing a drug at commercial scale. Molecules can and do adopt more than one type of crystal structure upon precipitation.

The Thermo Scientific iCAP 6000 Series ICP-OES and Thermo Scientific iTEVA Software are ideal for the analysis of trace elements in pharmaceutical products.

To date, we’ve experienced a year of mega-mergers with six of the top pharmaceutical players combining forces to become three major contenders. What does this mean for the affected employees and managers alike? Well, believe it or not, it can lead to employment opportunities and personal successes that otherwise may not have been considered.

As more therapeutic proteins enter the market, an even larger number accumulate in biopharmaceutical drug pipelines. In order to improve assay quality and manage the growing workload, automated systems are needed to provide qualitative and quantitative information.

Like other new tools in the drug discovery process, automation, implemented properly, can generate the insight necessary to drive the pharmaceutical business forward.

The FDA has increased its focus on modernizing the regulation of pharmaceutical manufacturing and drug product quality. As a result, innovative pharmaceutical companies are re-examining whether traditional drug development and commercialization processes are sufficient.