Chromatographic method validation is a critical step in the workflow of pharmaceutical, food safety, chemical and environmental laboratories that can adversely impact regulatory compliance, product development, and ultimately, product release and availability.
The current validation process is time consuming and prone to errors, which can decrease laboratory productivity and increase the time and costs associated with bringing new and existing products to market.
Download this whitepaper to discover how Empower Method Validation Manager can streamline the chromatographic method validation process, with benefits such as:
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