Integra IT provides customized software development services in response to each client’s necessities and challenges in healthcare and clinical research. Our dedicated development team allows us to create, set up, and launch robust and customized tools in record time.
We have comprehensive experience in data management and processing at a country scale, successfully operating nationwide and multicountry-wide support.
Clinical trial follow-up from the beginning through the end
Registration of indicators, times, changes, and comparative analysis
Dynamic and reliable clinical studies record
Compare national or regional indicators with international ones
High-end technology with 100% serverless architecture and data safety standards
Affordable (accessible) for small and medium size Sites, CROs, and Sponsors
Real-time data for data-driven decisions
Faster start-up studies
Interoperability (integrations between own and third-party systems)
Validated and GCP-compliant
On-demand scalable architecture (per solutions, modules, and features)
Expertise in low and middle-income countries
Vaccine-exclusive features available
Around 70% of our clinical research experts are Latin American professionals with global experience
The Metrics software is a tailor-made tool that enables the user to record and control clinical trial development for countries, local authorities, and associations, aiming for time management in a unified database. Check trial status, establish key indicators for effective decision-making and optimize resources and efforts strategically to make the local clinical trials field more competitive and efficient.
Currently, the Metrics solution is being used by the most important pharmaceutical, I&D, and research organization in Colombia (AFIDRO), contributing to clinical research development and improving tracking trial progress. Likewise, having this kind of tool helps to attract investment and find new ways to promote clinical research initiatives in middle and emerging markets.
Integra IT.
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.
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Other Solutions.
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About us.
