We disrupt the market thanks to our advanced methodology, which includes:
1. Emerging markets experience
EDC systems and Data Management already deliver efficient clinical trials worldwide. However, Low and Middle-income countries still need more access to developing these capabilities; therefore Integra IT model is based on cost-convenient and high-end technology, close customer support, and an in-house team of qualified medical experts, engineers, and high-skill professionals from Latin America.
2. Technology featuring services, all-in-one
We combined top data engineering systems with complementary professional services to deliver a customized approach to each client, doesn’t matter if it is a small RWE study or a large vaccine clinical trial. Our technical team is agile and fast, even in the most complex trials and protocol designs.
3. Interoperability
Under our equity and access-for-everyone principle, we perform seamless integrations with our own and third-party systems. We integrate our EDC with Electronic Medical Records (EMR/eSource), electronic patient-reported outcomes ePRO/eCOA systems, and/or third-party systems in record time. We use API integrations and on-cloud storage to mitigate incompatibility, team burden, and lack of standardization. For each project, we ensure high-quality standards, compliance, and safety, following data protection regulations (GDPR).
4. Analytics and reports
5. eCRF software usability
Integra IT has developed an intuitive interface for all the study team. Based on the role, the interactions, alerts, icons, graphics and more, are designed to be user-friendly and decrease the adoption curve time.
6. CDISC Standards
Data is by default in CDASH standard and our EDC/eCRF system embeds an automated feature to transform data from CDASH to SDTM when needed and data is also exported in several common extensions such as SAS, xls and CSV.
Talk with one of our medical experts and let us exceed the expected outcomes for your next clinical trial
