NUES, Inc.
Established in 2017, NUES Inc is a niche contract research organization (CRO) serving medium-to-large corporations and federal government agencies. Services focus on regulatory and clinical development support, public health research, educational research, project management, and custom solutions with attention to work in emerging countries.
Industries
N/A
Services
Clinical Development
Regulatory and clinical services for investigational drugs and medical devices, including regulatory strategy, clinical operations support and submission publishing.
eCTD Publishing and Submissions
Compilation, validation and electronic submission of regulatory dossiers.
Pharmacovigilance and Drug Safety
Safety surveillance and post-marketing safety services.
Public Health Research Services
Epidemiology, data collection and management, global health initiatives, program analysis, implementation and evaluation, and health equity research.
Educational Services and Research
Education research, program planning, policy analysis, STEM education initiatives and statistical methodology.
Project Management and Consulting
Project and program management across product life cycle, operations support, and bespoke consulting engagements.
Clinical Development
Regulatory and clinical services for investigational drugs and medical devices, including regulatory strategy, clinical operations support and submission publishing.
eCTD Publishing and Submissions
Compilation, validation and electronic submission of regulatory dossiers.
Pharmacovigilance and Drug Safety
Safety surveillance and post-marketing safety services.
Public Health Research Services
Epidemiology, data collection and management, global health initiatives, program analysis, implementation and evaluation, and health equity research.
Educational Services and Research
Education research, program planning, policy analysis, STEM education initiatives and statistical methodology.
Project Management and Consulting
Project and program management across product life cycle, operations support, and bespoke consulting engagements.
Expertise Areas
- Clinical trial management
- Regulatory strategy and submissions
- Pharmacovigilance and safety surveillance
- Clinical data management
Key Technologies
- eCTD electronic regulatory submissions
- ClinicalTrials.gov and EudraCT data management
- Computer-aided drug design (CADD)
- PK/PD modeling