It offers full service Phase II–IV CRO solutions, combining clinical expertise with efficient execution to support drug development from concept to approval. With a strong foundation in clinical pharmacology and early stage studies, we manage trials across various therapeutic areas, including oncology, dermatology, and respiratory. Our services cover everything from trial design and project management to safety, data management, and regulatory submissions. As the only U.S. CRO licensed for dermal Open Flow Microperfusion (dOFM) studies, we provide specialized capabilities alongside comprehensive operational support to ensure high-quality, timely results.
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