Let Ascenth streamline your Clinical Trial by managing every Aspect of it. The key elements include:
- Site Management
- Site selection. We have a vast network of sites all over United States which are high performing and strictly follow GCP guidelines. The sites have rapid start up and produce quality data.
- Develop a recruitment strategy
- Support regulatory submission to local/central IRB
- Develop Site Monitoring plan
- Review site performance
- Logistic support
- Quality Management
- Oversee the Data Management and Biostatistics
- Manage Trial Master File
- Laboratory Integration and Management
- Vendor management
- Medical writing
- Open and transparent communication with sponsor