Integra IT is the best partner for clinical trials. We are specialized software and application development company focused on the process optimization and improvement of clinical trial operations. Beyond digital tools, we give our partners trust through data safety, quality, and timely support for their projects. This aims to achieve science-proof outcomes that benefit people’s life.
Since 2009 we have been improving part clinical trial execution in more than 15 therapeutical areas, including COVID-19, phase I to IV, and RWE. We have the trust and results of the CRO and sponsors in over 18 countries worldwide, with extensive experience in clinical trials in emerging markets.
Integra IT’s multidisciplinary team is trained to understand and analyze the needs of each site and CRO according to each clinical trial objective. From end-to-end, we make data gathering more efficient through technology, making the process user-friendly for staff and patients, and always protected under the best quality standards from GCP and the FDA 21 CRF Part 11.
We deeply understand the purpose of each clinical trial: to improve people’s quality of life. This is why we strive to deliver innovative products, such as TrialPal, which gather electronic diary information and make detailed surveillance of the participants. On the other hand, Trial360, our all-in-one software solution for Sites, includes an Electronic Medical Record, centralizes the data, and integrates with recruitment, scheduling, management, laboratory sample internal management, and resource allocation of a clinical trial according to the protocol. Sponsors and CROs can benefit from our TrialPal or Trial360 automatic integration to any EDC or to our own eCRF, which includes IRT, SAEs reports as well as database cleaning, analytics, and data management services.
These are just a few of our suite of software solutions, to get to know more about them and how they work, schedule a meeting with us for a demo at:
