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.
Our
value proposition.
Propuesta de Valor.
We understand and listen to participants.
Our experience in emerging markets has taught us how to increase patient engagement, maintain high adherence and reduce drop-out rates by understanding people's culture, context, technology literacy, and language.
We work in real-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.
Data privacy
and quality is our priority.
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.
We have significant experience.
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.
Our locations & Experience
Subjects
61000+
Countries
21+
Sponsors
20+
Diseases
20+
100% Satisfactory FDA Inspections
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.
Our principles
Person-Centered
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
On the cloud
We aim for CO2 reduction with 100% digital and web-based solutions; thus reducing paperwork, duplicate work for staff and mitigating human errors.
Compliance
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.
Customization
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.
News & Resources
How Rising Operating Costs in 2024 Are Impacting Clinical Research Sites in Latin America
The financial sustainability of clinical research sites in Latin America is facing one of its most significant challenges: the rapid and persistent increase in operating..
22 de December 2025
The Most Underfunded Budget Categories and How to Negotiate Them Successfully: Insights from the 2025 LATAM Landscape Survey
The Most Underfunded Budget Categories and How to Negotiate Them Successfully: Insights from the 2025 LATAM Landscape Survey
15 de December 2025
Accounts Receivable >90 Days: The Biggest Financial Risk for Clinical Research Sites in LATAM (Based on the 2025 Landscape Survey)
During the Ambassador Buenos Aires 2025 event, the Society for Clinical Research Sites (SCRS) presented the findings of the Latin American Landscape Survey 2025—a comprehensive...
9 de December 2025
Testimonials
At Integra IT, we found a novel and differential focus to lead our clinical trials. Their Trial Pal App has allowed us to improve the adherence and quality of the reported information from our participant subjects. We have formed a solid team with their Operations and Customer Service area, which allowed us to work hand in hand on developing and adapting Integra IT solutions to our needs.Integra IT brings us a complete approach, allowing our team to have information on time for better decision-making.
We were struggling with remote review and paper trails in our trials and research centers in Mexico. Integra IT's Trial360 saved our day!. Now we review activities remotely, improve data quality, since we have access to real-time information and collaborate with sponsors and workteam seamlessly We have formed a solid team with their Operations and Customer Service area, which allowed us to work hand in hand on developing and adapting Integra IT solutions to < our needs.Integra IT brings us a complete approach, allowing our team to have information on time for better decision-making..
At Integra IT I found many options to improve my process in any clinical trial..
We used to do most of our process on paper, adherence and follow-up in extensive studies were alwavs a big challenge. Thanks to Intera I platforms. we can easiv follow all study subiects.
We used to manage the subject's schedule in Excel but we had to keep a notebook apart to know when each subject came. It was a complicated process.Now thanks to the subject scheduling module we can have a better track of each subject in real time. Protocol deviations were reduced drastically!
The TrialPal Mobile App enabled us to continuously collect a large number of data sets from our study participants at a high frequency. Thanks to the Integra IT team, which reacted quickly and flexibly in a pandemic situation and created interfaces to our study systems in order to optimally integrate the app into our processes. Together, good progress has been made in vaccine development.
Our Clients
Are you looking for a more efficient clinical trial?
estudios clínicos más
eficientes?
Join our Partnership Program and get add-on services, complementary solutions, and investment in R&D. Such as Trialpal MoVi.
soluciones complementarias e inversión en I&D. Como Trialpal MoVi.