Product Overview
Analytical & Stability Services
We offer comprehensive analytical services to ensure the safety, quality, and compliance of your clinical and commercial drug products. With fully equipped on-site cGMP analytical and microbiological laboratories, including stability chambers, we provide thorough end-to-end quality control analysis, helping minimize risks and maintain timeline consistency. Our capabilities span a wide range of testing methods, including gas chromatography, HPLC/UPLC with advanced detectors, capillary electrophoresis, sterility testing, rheometry, and ICH-compliant stability studies, ensuring rigorous data integrity and reliable results. For complex projects, we specialize in analytical method development, validation, and testing for hard-to-analyze sample matrices, including viscous and reactive materials with limited stability. From early-stage development through commercial production, our collaborative QbD approach ensures your drug products meet critical regulatory requirements and deliver a stable shelf life, giving your company the confidence to move forward in even the most challenging applications.
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