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?
Statistical Design and Analysis
From protocol design and pre-study feasibility, to reporting, DSMB support and manuscript preparation.
Protocol Development and Data Management
From protocol document review to enable consistency, completeness and clarity, to site support, data cleaning and quality control.
Investigator, Site and Patient Services
From site identification, selection, activation, and monitoring, to patient recruitment, screening, blinding and management, we have the support services needed for your trial.
Join us where collaboration between scientists, clinicians, biostatisticians, data scientists, and IT experts is producing the highest quality results.
Pharmacovigilance and Medical Monitoring
Medical review and consultancy along with case processing, safety reporting, analysis, and submissions.
Regulatory Affairs Support
From strategy to implementation; from country and site-level regulatory authority applications, to document preparation and submission of CTA’s, IND’s, NDA’s, and BLA’s.
Medical Writing
Including protocols for both interventional and non-interventional trials, data management plans, study reports, manuscripts, posters and presentations.
Quality Assurance
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.
