It provides advanced bioanalytical services that support pharmacokinetic and pharmacology studies from Phase I through Phase IV. Our FDA-audited, state of the art laboratory offers rapid, reliable analysis with the capacity to process over 15,000 samples per month. Fully integrated with our clinical unit, we deliver expedited results for earlyphase studies, helping sponsors accelerate development timelines. Our team ensures all methods meet global regulatory standards, and we offer seamless coordination with CROs and clinical sites for late stage trials, maintaining full compliance and data integrity throughout.
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