Fostering Quality from Clinical Trials Through Commercialization.

With operational flexibility to provide development assistance on a stand-alone or an integrated full-service solution, our client’s specific needs are met with timely delivery and a unified partnership. From start-up Biotech to large Pharma and Medical Device companies, USDM Life Sciences Clinical Services and Solutions can facilitate and manage projects that span the entire clinical trial lifecycle. Our Clinical Subject Matter Experts specialize in GCP Compliance and Quality Assurance, Quality Systems, Data Management, Biostatistics and Programming, Drug Safety and Pharmacovigilance, as well as Medical Writing.

Areas of Focus

For Clinical/R&D

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Thought Leaders

Leading experts

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