At KYAMCH-BRS, we deliver high-quality data management and biostatistics services, ensuring confidence in your data throughout the drug development process. Our approach is responsive, flexible, and knowledgeable, with each study conducted with your goals in mind. Our Data Management team enhances efficiency, reduces development costs, and anticipates data risks.
Data Management
We deliver quality data with integrity. Our team collaborates with sponsored project teams to create detailed plans for clinical trial data collection, organization, validation, and analysis. We ensure a cost-effective, secure, and regulatory-compliant data management process. Trusted by sponsors, our extensive knowledge and experience are combined with superior therapeutic and regulatory expertise. Our robust data collection, validation, and analysis processes prioritize precision and efficiency while maintaining the highest levels of data quality and integrity.
Our expert team help you in:
- Design case report forms (CRFs) following standard regulations.
- Performs data entry of paper CRFs,
- Validates all project-specific components of the data management system,
- Reviews clinical data for errors and trends,
- Reconciles serious adverse events,
- Produces real-time clinical trial metrics,
- Data Safety Monitoring Board (DSMB) support.
