Emmes offers a robust suite of services for your Phase I-IV clinical trials, registries, observational studies and other clinical research.
What can we do for you?
Including protocols for both interventional and non-interventional trials, data management plans, study reports, manuscripts, posters and presentations.
Ensuring operations follow established procedures through auditing of study data, sites, laboratories, 3rd party vendors and CROs.
We look forward to talking with you, learning more about your specific goals and determining how we can help you.