The best cost-benefit eCRF/Electronic Data Capture (EDC) easy-to-set web solution in the market. Combined with our TriaPal ePRO/eCOA mobile solutions and Data Management capabilities, our services excel in deliverables, timing, and quality.
We foster high levels of efficiency, ensuring transparency, data integrity, and data quality.
The person in charge of entering the information will have the Data Entry role. This role can:
The CRA is the person in charge of verifying and managing queries. This role can:
The principal investigator verifies the information and signs it for approval. This role can:
Investigators and CRAs can generate the following surveillance reports to see how the trial is progressing:
Predefined Reports:
Administrators can also create personalized reports for delegated queries to allow for effective tracking. These reports can be set up at any stage of the trial, on an on-demand basis, and at no additional cost.
Surveillance Reports:
Investigators and CRAs can generate the following surveillance reports to see how the trial is progressing:
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At Integra IT, we use innovation in technology for data gathering, access, and surveillance in life science trials across all phases in an efficient manner. We offer a complete portfolio of 100% cloud solutions in compliance with GCP and FDA 21 CFR Part 11 regulations, aiming to make our partner’s work easier and more effective. We develop dedicated solutions for pharmaceutical companies, CROs, and sites.
