The clinical data management landscape is rapidly changing. As data volumes explode from diverse sources like wearables, EHRs, and remote patient monitoring, the industry faces new challenges in data integrity, security, and regulatory compliance. The focus has shifted from simple data entry to comprehensive clinical data science, where the ability to integrate, harmonize, and analyze complex datasets at scale is critical for ensuring patient safety and accelerating trial timelines.
This new era of clinical trials demands a forward-looking approach. The key to success lies in organizations using AI and automation to bridge the gap between messy, siloed data and high-impact decision-making. From patient-centric data collection to the use of advanced analytics for real-time data monitoring and risk-based quality management, the future of clinical research is being shaped by those who are data-ready.
Elucidata helps clinical research teams make that leap. Our AI-powered data solutions streamline the entire data lifecycle, from ingestion and harmonization to analysis and submission. Our Senior Scientific Manager, Shubhra Agrawal, will be at SCDM 2025 to share how we’re solving one of the biggest bottlenecks in clinical trials: getting clinical data clean, contextualized, compliant, and AI-ready at scale.
1. Data Interoperability as a Service: 6X Faster Clinico-Genomic Data Integration & Analysis with Polly
2. Elucidata Speeds Drug Toxicity Insights 4X by Integrating Clinical and Omics Data
3. Real-Time Data Quality Assessment with Elucidata's Polly
4. Elucidata Scales Clinical Data Extraction 8x Faster from Hospital Records than Manual Method