ARS EDC/ ARS eCRF

ARS EDC stands for Electronic Data Capture by Advance Reporting System powered by Yuva Infocare Pvt Ltd, which is a computerized system used in clinical trials to capture, manage, and report clinical trial data. ARS EDC replaces traditional paper-based data collection methods, making the process more efficient and accurate.

ARS EDC/ ARS eCRF dashboard

ARS EDC system allow for the electronic collection of clinical trial data, which can be entered directly into the system by the investigator or study coordinator, or through direct data capture from medical devices. ATS EDC system typically have features such as data validation and real-time data monitoring to ensure the accuracy and completeness of the data collected.

Some features of ARS EDC systems include

Electronic case report forms (eCRFs)

ARS EDC system use electronic forms to capture data from clinical trials, which can be designed to match the specific needs of the study.

Data entry

ARS EDC systems provide electronic forms for entering data, replacing traditional paper-based forms.

Role-based access control

ARS EDC systems can provide role-based access control, ensuring that only authorized users can access and modify study data.
ARS EDC system use electronic forms to capture data from clinical trials. These forms can be customized to match the specific needs of the study, including the types of data to be collected and the format of the data.

Data monitoring

ARS EDC systems can monitor data entered into the system, alerting users to any data discrepancies or missing data. ARS EDC systems can provide real-time monitoring of study data, allowing for early identification of data anomalies or protocol violations. This can help reduce the risk of errors and ensure compliance with study protocols.

Data validation

ARS EDC systems can automatically validate the data entered into the system, ensuring that the data is accurate and complete. This can help reduce errors and improve the quality of the data collected.

Remote monitoring

ARS EDC systems can enable remote monitoring of study data, allowing sponsors and monitors to access study data securely from anywhere in the world. This can help reduce the time and cost associated with on-site monitoring visits.

Audit trails

ARS EDC systems can track changes made to data, providing a record of who made changes and when they were made. ARS EDC systems can provide an audit trail of all data changes, ensuring that the data is traceable and secure.

Data export

ARS EDC systems can export data in various formats, making it easy to share data with other researchers or regulatory agencies. This can facilitate the analysis and interpretation of study data.

eCRF cro staff
eCRF Model

Overall, ARS EDC systems provide a more efficient and accurate way to collect and manage clinical trial data. They can improve data quality, reduce data entry errors, and provide real-time data monitoring, making them an essential tool for clinical trial management.

ARS EDC systems provide a powerful tool for the collection, management, and analysis of clinical trial data, improving efficiency, accuracy, and compliance in clinical research.