This case study highlights our groundbreaking work with a leading international Contract Development and Manufacturing Organization (CDMO) specializing in injectable solutions. Our mission was to optimize and automate analytical methods using Ultra-High-Performance Liquid Chromatography (UHPLC), a project that promised to elevate quality control standards to unprecedented levels.
Key Achievements
- Mastery of Empower 3 software for advanced UHPLC analytics.
- Development of new automated calculation formulas, reducing analysis time from over a day to 30 minutes to 1 hour.
- Comprehensive overhaul of analytical records, enhancing clarity and reducing analysis review time significantly.
Impact
The automation of UHPLC analytics brought about a transformative leap in the efficiency and precision of quality control processes within the pharmaceutical industry. By significantly reducing the time and potential for error in UHPLC analysis calculations, our project not only streamlined operations but also freed up valuable resources, allowing for more focus on innovation and development. This initiative marks a paradigm shift towards a more efficient and error-resistant approach to pharmaceutical quality control.
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