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White Paper

Traditional methods for steroid quantification often involve cumbersome processes that are prone to human error, leading to inconsistent results and extended turnaround times. 

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The need to comply with stringent regulatory standards adds another layer of complexity, demanding meticulous documentation and validation procedures to ensure the accuracy and reliability of test results.

This comprehensive white paper demonstrates a targeted solution to these common problems, helping clinical lab managers enhance operational performance while upholding high standards of patient care, empowering lab managers to tackle these challenges head-on. 

Steroid quantification is particularly challenging due to the inherent variability in biological samples, the presence of interfering substances, and the need for highly sensitive and specific detection methods. These issues can lead to inaccurate measurements, which can compromise patient care and diagnostic outcomes. Additionally, existing methods may require extensive manual intervention, which not only slows down the workflow but also increases the risk of errors.

Download the full white paper to learn how an LC-MS steroid panel improves reliability and efficiency of steroid analysis in clinical diagnostics through a method comparison between an in-house method and commercially available CE-IVD kit solution.