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What we do
At Integra IT, we’re on a mission to expand clinical research possibilities worldwide, especially in diversity, inclusion, and emerging countries. Our comprehensive software ecosystem is cost-convenient and high-efficient for all clinical research stakeholders.
Integra IT’s fully flexible and scalable tech solutions and services enable clinical trials end-to-end control and visibility. Thanks to our software agile engineering and clinical operations expertise, we can streamline clinical trials and make deployments in record time.
Make decisions in real-time and manage your KPI effectively; get an overview of your clinical trial, real-world evidence (RWE), or observational study in dashboards for tighter control.
We develop solutions with high-security and quality control standards. We guarantee data integrity with ICH-GCP, 21 CFR Part 11, GDPR, EU ANNEX 11, ALCOA and HIPAA regulations.
With our experience in 17 countries and 17 different therapeutic areas (specially in vaccines trials such as: covid 19, chikungunya, polio and 10 more) we have excelled in getting clinical trials to the next level since 2009; our expertise in high-end and person-centered technology has led us to game-changing software solutions for each and every stakeholder.
Make decisions in real-time and manage your KPI effectively; get an overview of your clinical trial, real-world evidence (RWE), or observational study in dashboards for tighter control.
Since 2009 we have excelled in getting clinical trials to the next level; our expertise in high-end and person-centered technology has led us to game-changing software solutions for each and every stakeholder. We have experience in 18 countries and 17 therapeutics areas
At Integra IT, we provide technological tailored solutions to help pharmaceutical companies, CROs, and investigation sites to succeed in the performance of clinical studies (phase I – IV). We offer a complete portfolio of 100% cloud solutions in compliance with GCP, FDA 21 CFR Part 11, EU Annex 11 and HIPAA regulations, aiming to make our partner’s work easier and more effective.
We understand the culture and reality of each emerging country; we know having presence and support on-site, in the same language is essential for a great outcome.
We aim for CO2 reduction with 100% digital and web-based solutions; thus reducing paperwork, duplicate work for staff and mitigating human errors.
Our solutions are developed in compliance with ALCOA, GCP, EU ANNEX 11, ICH-GCP and 21 CFR Part 11 guidelines and standards. Our audit trail guarantee transparency among parts.
We offer modular and flexible software to be customized according to the client's needs. We listen and work closely with our partners to give them timely and precise responses to exceed their expectations.
Table of Contents “Utilizing ePROs not only facilitates better data collection but also contributes to improved quality of care and patient safety”. “FIdec achieved over
Table of Contents Adherence to Good Clinical Practices (GCPs) is mandatory in clinical trials. These rigorous standards ensure safety, ethics, and reliability in medical research.
Table of Contents Utilizing CTMS can cut operational costs by about 25%, making clinical trials more cost-effective. This significant reduction in expenses allows research centers
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