Broad and precise operations with our eCRF and Data Management Services
Data move us! Our eCRF & Data Management Services gives clinical trials a broad and precise operations control under one integrated platform. We have vast
May 13, 2022
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:
Enroll
Subject
Enter
Data
The CRA is the person in charge of verifying and managing queries. This role can:
Verify
Information
Manage
Queries
Electronic Signature
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:
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.
Affordable (accessible) for small and medium size Sites, CROs, and Sponsors
Real-time data for data-driven decisions
Faster start-up studies
Interoperability (integrations between own and third-party systems)
Validated and GCP-compliant
On-demand scalable architecture (per solutions, modules, and features)
Expertise in low and middle-income countries
Vaccine-exclusive features available
Around 70% of our clinical research experts are Latin American professionals with global experience
Data move us! Our eCRF & Data Management Services gives clinical trials a broad and precise operations control under one integrated platform. We have vast
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Integra IT.
At Integra IT, we use innovation in technology for data gathering, access, and surveillance in life science studies across all phases in a time-reliable manner. We offer a complete portfolio of 100% cloud solutions in compliance with GCP, FDA 21 CFR Part 11, Annex 11 and HIPAA regulations, aiming to make our partner’s work easier and more effective. We develop tailored solutions for pharmaceutical companies, CROs, and sites.
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