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What we do
At Integra IT, we use innovation in technology for data gathering, access, and surveillance in life science trials across all phases efficiently. 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.
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, 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 18 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 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 customised according to the client needs. We listen and work closely with our partners to give them timely and precise responses to exceed their expectations.
The clinical trial of the polio vaccine was critical for the emergency approval of the M5 sponsor vaccine against the second wild strain, thus solving
According to the American Agency for Healthcare Research and Quality (AHRQ), an EMR system is defined as “an electronic record of health-related information on an
Dr. Jose Jimeno en TEDx Amador TEDX Amador llevado a cabo en el Teatro Pacific, fue una iniciativa de la Asociación de Estudiantes de Medicina
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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.
