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
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