Building a Strong Foundation: Robust Metadata Repository (MDR) Framework for Automated Standard Compliant Data Mapping
Pharmaceutical and biotechnology companies operate within a constantly evolving regulatory landscape, where adherence to standards set by organizations like the Clinical Data Interchange Standards Consortium (CDISC) is crucial for submitting clinical trial data. In the area of clinical trial data management, information can originate from various sources and be stored across different platforms, systems, and […]
