Data Inaccuracy and High Costs: Manual data entry errors necessitate costly verification processes, with source data verification (SDV) alone potentially accounting for up to 20% of the clinical study budget.
Time Constraints: Delays in data collection and verification extend clinical trial timelines, slowing down the time to data lock and study completion.
Regulatory Compliance and Resource Management: Ensuring data meets regulatory standards is complex and resource-intensive, while the need for qualified staff doing tedious tasks leads to inefficiency and high turnover rates.
Archer cuts the time to receive site data by half, offering the potential to speed up clinical studies. This boosts data analysis, decision-making, and can accelerate the speed to database lock, ultimately shortening time to market.
Archer functions exclusively as a data processor, ensuring that no personally identifiable information (PHI) is retained or stored, thus providing top-tier data security. Our platform also includes comprehensive auditing capabilities for transparency and peace of mind.
Sponsor-Centric Benefits: Archer's SMART on FHIR technology streamlines data integration from EHRs to sponsors' EDCs, speeding up trial management and reducing costs.
Optimized Resource Allocation: Archer automates data collection and verification, allowing sponsors to manage multiple trials without increasing resources. This reduces manual tasks, saving time and money.
Enhanced Data Quality: Archer captures data directly from EHRs, minimizing manual errors and improving data quality. This helps sponsors make faster, more accurate decisions and reduces delays.
Increased ROI: Archer improves site efficiency and data accuracy, with the potential of saving up to $15,000 per patient in a clinical trial.
Transform your clinical trials with Archer’s unparalleled accuracy and efficiency visit our website, request a demo, or contact us at sales@ignitedata.com to learn more.
