Manual Data Entry: Sites face high error rates and inefficiencies due to manual data transcription.
Resource Intensive: Significant time and staff resources are required for data verification and management.
Regulatory Compliance: Ensuring data accuracy and compliance with regulatory standards is complex and time-consuming.
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.
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.
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.
Site-Friendly: Archer’s intuitive design eases manual data entry, boosting adoption and satisfaction among site staff.
Resource Efficiency: Archer automates data tasks, enabling sites to manage more trials with existing resources, optimizing staff and infrastructure.
Staff Retention: By minimizing tedious tasks, Archer enhances job satisfaction, reducing staff turnover.
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.