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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.
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 17 countries and 17 therapeutics areas.
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
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.
Vaccine clinical trials are very complex, around 12 years are needed between Phase I and Phase III studies until a license can be achieved, and
In recent years, sites have increasingly invested in technology to eliminate paper records and reduce workloads related to inputting data, scanning, and transcription. Even though
Investigator-Initiated Studies (IIS) are studies where an individual investigator, a research site, or a group of research sites carry out the research from the protocol
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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.
For Sites.
Other Solutions.
For CROs.
About us.
