Trial
NICR can provide clinical trial monitoring for your organization.
With a team of fully-trained professionals, we can manage your clinical trials from start-up through phase II-IV trials.
We also offer complete training and ongoing support for new physicians and study coordinators.
The NICR Advantage
To deliver effective clinical trial programs, NICR will:
- Implement ongoing site training
- Reduce patient drop drop-out rates
- Increase patient enrollment rates
- Enable the expansion of projects to a large pool of potential patients
- Build robust databases for future research projects
- Deliver high-quality data
- Process specimens complete and core laboratory procedures
- Increase site participation in clinical trials
- Provide of variety of clinical research experience
- Integrate systems and services to eliminate clinical trial delay
- Support and enhance central and local IRB interactions
- Distribute safety reports through a tracking and monitoring systems
We Manage Trials
- Implement ongoing site training
- Reduce patient drop drop-out rates
- Increase patient enrollment rates
- Enable the expansion of projects to a large pool of potential patients
- Build robust databases for future research projects
- Deliver high-quality data
- Process specimens complete and core laboratory procedures
- Increase site participation in clinical trials
- Provide of variety of clinical research experience
- Integrate systems and services to eliminate clinical trial delay
- Support and enhance central and local IRB interactions
- Distribute safety reports through a tracking and monitoring systems