What can we do for you?
Emmes CRO possess experience across a broad range of therapeutic areas, with specializations in Vaccines and Infectious Disease, Ophthalmology, Clinical Neuroscience, Rare Disease, Cell and Gene Therapy and Government.
Clinical Research Services
Emmes offers a robust suite of services for your Phase I-IV clinical trials, registries, observational studies and other clinical research.
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.
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Protocol Development and Data Management
From protocol document review to enable consistency, completeness and clarity, to site support, data cleaning and quality control.
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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.
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Statistical Design and Analysis
From protocol design and pre-study feasibility, to reporting, Data and Safety Monitoring Board (DSMB) support and manuscript preparation.
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Global Regulatory Affairs
Emmes can help you navigate the investigational new drug, device and biologics regulatory pathways toward a successful product launch.
Read moreLearn more about our cloud-based suite of applications for study design, data capture, randomization and reporting.
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Let's discuss how our clinical research expertise can support your next study.
- Speak with a clinical research expert
- Tailored solutions for your study needs
- Quick and easy scheduling
Resources
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