Real-Time efficiency and sharp insights with oomnia eCOA

• oomnia eCOA allows to manage time series data, such as continuous monitoring data from wearables or sensors, crucial for understanding patient states over time

• oomnia eCOA supports various types of surveys and questionnaires, including adaptive questionnaires that change based on previous responses

• oomnia eCOA supports both structured data (like forms, checklists) and unstructured data (like physician's notes, free-form patient feedback)

• oomnia eCOA can integrate and handle biomarkers, which are becoming increasingly important in personalized medicine and complex trials

• oomnia eCOA allows to manage time series data, such as continuous monitoring data from wearables or sensors, crucial for understanding patient states over time

• oomnia eCOA supports various types of surveys and questionnaires, including adaptive questionnaires that change based on previous responses

• oomnia eCOA ensures data is captured and stored in standardized formats, facilitates data pooling and analysis across different trials or studies

• Automation of certain processes and the generation of alerts for important events or inconsistencies in data through oomnia eCOA improves efficiency and data reliability

• oomnia eCOA has an advanced and crucial ability to customize data capture methods and forms to suit specific trial requirements

• oomnia eCOA provides real-time data access and analysis which allows for timely decision-making and improves the management of the clinical trial

• oomnia eCOA ensures data is captured and stored in standardized formats, facilitates data pooling and analysis across different trials or studies

• Automation of certain processes and the generation of alerts for important events or inconsistencies in data through oomnia eCOA improves efficiency and data reliability

• oomnia eCOA ensures data accuracy and consistency across platforms
• This includes validation checks, audit trails, and standardized data formats

• Regular quality checks and assurances to maintain data integrity and compliance are essential

• The ability to access and analyze data in real time is crucial
• oomnia eCOA enables timely decision-making, monitoring of patient safety, and adaptive trial management

• oomnia eCOA provides advanced analytics and reporting tools to help in data interpretation, trend analysis, and generating insights

• oomnia eCOA ensures data accuracy and consistency across platforms
• This includes validation checks, audit trails, and standardized data formats

• Regular quality checks and assurances to maintain data integrity and compliance are essential

• Active participation is achieved by direct patients and physicians data report through familiar electronic devices like smartphones, tablets, or web-based platforms
• No setup required for our web-based platform, and BYOD (Bring Your Own Device) is easily achievable

• Efficiently manage and streamline communication between participants, site staff, and trial management, enhancing the overall coordination of clinical trials

• oomnia eCOA has a convenient interface, making it easy for participants to enter data, understand instructions, and comply with the study requirements
• This can improve the accuracy and consistency of patient-reported data

• Features that promote participant engagement, like interactive tools, educational materials, and personalized communication, can help in retaining patients throughout the trial duration

• Active participation is achieved by direct patients and physicians data report through familiar electronic devices like smartphones, tablets, or web-based platforms
• No setup required for our web-based platform, and BYOD (Bring Your Own Device) is easily achievable

• Efficiently manage and streamline communication between participants, site staff, and trial management, enhancing the overall coordination of clinical trials

• oomnia eCOA complies with relevant regulations such as HIPAA, GDPR, Swiss Data Privacy Law, FDA 21 CFR Part 11, and EMA EU GMP Annex 11

• Strong user authentication mechanisms and role-based access controls to ensure that only authorized personnel can access or modify sensitive data

• Both in transit and at rest, all data is encrypted
• This ensures that sensitive participant and trial data is protected from unauthorized access

• Features ensuring data integrity, such as range checks for data entry, validation of data formats, and checks against data tampering
• Data transfer suiting industry standard HL7 and FHIR protocols

• oomnia eCOA complies with relevant regulations such as HIPAA, GDPR, Swiss Data Privacy Law, FDA 21 CFR Part 11, and EMA EU GMP Annex 11

• Strong user authentication mechanisms and role-based access controls to ensure that only authorized personnel can access or modify sensitive data

• oomnia eCOA is flexible enough to accommodate different trial designs and protocols
• This includes the ability to handle various types of data, from subjective patient-reported outcomes to objective clinical assessments

oomnia eCOA is an electronic Clinical Outcome Assessment platform that enables participants and site staff to report data directly using electronic devices. It improves data collection by enhancing accuracy, speed, and engagement in clinical trials.

Key features include real-time data integration with our EDC, RTSM, and CTMS, a user-friendly interface, enhanced participant engagement, streamlined communication, simplified document management, and compliance with regulatory standards.

Real-time data integration allows for immediate updating and centralization of trial data within our oomnia EDC and CTMS system, significantly improving management, efficiency, and decision making, while reducing costs and human resources for clinical trials.

In order to book a demo call with an oomnia expert, simply press the button below, select a date in the booking tool and fill in all necessary information. After that, we will send you an invitation.