EP Series
EP Series™ is a solution for the centralized GLP-compliant management, analysis, simulation and reporting of PK/PD laboratory data in drug development. The system was developed in conjunction with several major pharmaceutical companies to ensure it meets the real-world needs of Scientists, Quality Assurance personnel, and Information Technology staff in pharmaceutical, biotech and other research organizations. The EP Series provides Laboratory Information Management (LIMS) capability for PK/PD laboratory data and integrates with Kinetica™, WinNonlin™, NONMEM and SAS to integrate information into Enterprise-Wide Knowledge.
Product Detail
Benefits
- Accelerated study report generation
- Reduced costs associated with data management
- Packaged Integration, extraction and transformation of external data
- Flexible Data exchange with third party products
- Study reconciliation and traceability
- Regulatory compliance with GLP and 21 CFR Part 11
Key Features
- Flexible Study Structure Design
- Data Exchange And Import
- Seamless Data Extraction, Transformation and Transfer
- Comprehensive Data Analysis
- Powerful Reporting
- Robust Security and Regulatory Compliance
- EP Applications
Product Detail
Benefits
- Accelerated study report generation
- Reduced costs associated with data management
- Packaged Integration, extraction and transformation of external data
- Flexible Data exchange with third party products
- Study reconciliation and traceability
- Regulatory compliance with GLP and 21 CFR Part 11
Key Features
- Flexible Study Structure Design
- Data Exchange And Import
- Seamless Data Extraction, Transformation and Transfer
- Comprehensive Data Analysis
- Powerful Reporting
- Robust Security and Regulatory Compliance
- EP Applications