An electronic Case Report Form is a digital version of the traditional paper-based Case Report Form (CRF) used to collect and record data during a clinical trial.
An eCRF serves as a standardised tool for capturing patient data, study-specific information, and clinical outcomes.
Your Research’s eCRF module is designed to capture various types of data, including demographics, medical history, laboratory results, adverse events, medication details, and other relevant information.Â
It provides a structured framework for data collection, ensuring consistency and accuracy in the data recorded across different study sites.
eCRF facilitates remote data entry, enabling researchers and site staff to enter data directly into the system from various locations.
Additionally, eCRFs can support data integration and interoperability with other clinical trial systems, such as electronic data capture (EDC) systems or electronic health record (EHR) systems.
eCRFs provide a structured framework for data collection, allowing researchers to define and capture specific data elements required for the study.
The form is designed with fields, checkboxes, dropdown menus, and other input options to ensure consistent and standardised data entry.
Structured data collection minimises errors and ensures uniformity across different study sites, facilitating data analysis and interpretation.
The Your Research eCRF system incorporate data validation checks and quality control mechanisms to enhance data accuracy and completeness.
These checks can include range checks, logic checks, and data consistency checks to identify errors or inconsistencies in real-time.
By implementing automated validation, our eCRF helps to reduce data entry errors, improve data quality, and save time by identifying and correcting issues promptly.
The Your Research eCRF module enables real-time data monitoring and remote access capabilities, enhancing the efficiency and convenience of data management in clinical trials.
Researchers and site staff can access the eCRF system remotely, securely enter data, and monitor data collection progress.
This feature facilitates timely data entry, reduces delays in data availability, and allows for proactive monitoring of data quality and compliance throughout the trial.
Help streamline your data collection process, improve data quality, enhance data management capabilities with Your Research’s eCRF module.
Your Research’s eCRF module provides structured data collection, data validation checks, and data consistency measures.
This helps improve the quality and accuracy of data collected during the trial.
By enforcing data entry rules and validation checks, it can reduce data entry errors, detect inconsistencies in real-time, and prompt corrections.
Your Research’s eCRF module streamlines data management processes in clinical trials. It enables efficient data entry, automated data handling, and real-time data monitoring.
Researchers and site staff can remotely enter data, reducing the need for manual data transcription and paperwork. The electronic format facilitates faster data collection, data cleaning, and data integration.
Your Research’s eCRF helps improve compliance with regulatory standards and guidelines in clinical trials.
The electronic format allows for easier adherence to data privacy and security requirements. eCRFs can implement access controls, audit trails, and encryption to protect patient data and maintain confidentiality.
Additionally, it supports traceability and documentation of data changes, promoting transparency and audit-ability.
Discover how our eCRF module optimises clinical trials and academic research, enhancing data collection and participant comprehension.
With Your Research, you have the flexibility to utilize stand-alone modules, integrate them with your existing software vendors, or connect them to other modules within Your Research to enhance the participant journey.
Contact us and we will be happy to show you how Your Research makes a difference in conducting clinical research, making research more efficient and personalised for everyone involved.