
Dartmouth-Hitchcock Research Administration provides dedicated space and staff for the efficient conduct of clinical research across the life cycle of a project. Research nurses and coordinators assist with study preparation, regulatory and IRB submissions, study procedures and sample processing according to protocol requirements.
Learn MoreDartmouth-Hitchcock Clinical Trials Office (CTO) supports initiation and conduct of high-quality clinical studies through investigator collaboration, contract/budget/MCA review, and regulatory support for GCP compliance.
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