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Deploy seamless integrations 

within proprietary or third-party systems​

Our eCRF, TrialPal & &PFS or Trial 360 combined

The combination of three of our best solutions is made to be an easy-to-use platform for your site's needs. Integrating our EDC, eCOA/ePRO, and trial management system is easy and seamless. Monitoring study participants and the study in general, minimizing processes, reducing costs, keeping track of diaries and registers, and monitoring the clinical trial data; all in one integration. For Integra IT, interoperability is a premise; we deliver fast and impeccable integrations with third-party systems like RAVE.

  • Trialpal ePRO/eCOA
  • Patien Follow Up System
  • Trial360 
  • eCRF  & Data Management system
  • With Third-part systems

Main Benefits of the Integration


All digital, less time, save money

Get close to your patient or subject



Customized stats


Completely secure and 21 CFR Part 11 Compliant


Integration Model



Below you will find an integration example. Our solutions include an easy-to-setup API that extracts data from our ePRO or eCOA to Site CTMS and, along with our eCRF Importer, is then transferred to our proprietary eCRF or a third-party study EDC system like RAVE. In the RAVE example, we use Rave Web Services to make both systems communicate with each other. We have also developed an integration checker that review and compares data between systems, so the research site can be confident that all data was transferred successfully and that data integrity is being met.


Notes: 

  • Integrations take 2-3 weeks depending (approx) on study forms (# variables, visits, e-Dairy days).
  • Testing and validation take one week (approx) to make sure integration works flawlessly.
  •  Rave dedicated user needed to authenticate transactions via RWS.

Integration Scheme Example

Accesible para

patrocinadores, CROs y

centros de investigación

pequeños y medianos

Por qué Integra IT

Información en tiempo

real para la toma de

decisiones basada en

datos


Soluciones

Soluciones validadas en

buenas practicas

clínicas y en

cumplimiento de

normativa internacional


Estudios con inicios

rápidos


Soluciones

interoperables entre sí e

integrables con

soluciones de terceros


Arquitectura escalable on-off a demanda


Experiencia en países de bajos y

medianos ingresos


Funcionalidades especiales para estudios

de vacunas