Solutions for Sites
From a Complete Vertical Life Science ERP to a simple to use Site CTMS and compliant EHR 
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Multiple Solutions for your site

From a complete vertical Life Science ERP to a simple-to-use scheduling system and clinical trial management system, including an Electronic Health Record design for clinical trials, that can also be integrated with the most popular eCRF or EDC such as RAVE from Medidata.

  • Trial 360 (a modular and complete Site CTMS and ERP)
  • PFS (Patient Follow up System)
  •  eCRF (Case Report Form System & Data Management Services) 
  • Integration Services and API (Between EDC, eCOA & Site CTMS)

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With an initial study discount!

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Our Services For Sites

We have created a set of services and solutions to help Sites adapt to a digital world and transform with the accompaniment needed to change and gain insight and control to comply with each clinical trial objective. We have learned that a happy Site is the basis of an outstanding and efficient study.


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Patient Follow-up System

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Integration Services

(EDC, eCOA & Site CTMS)

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We develop software as a service, take a look at how they work.


Trial 360

An All-in-one Ecosystem

Trial360 is a web based 21 CFR Part 11 compliant, easy to use platform, a vertical Life Science ERP and Site CTMS that speeds up processes and improves quality across the clinical study.


Patient Follow

up System


It is an intuitive and easy-to-use tool that allows monitoring of study participants and the study in general.

It is a configurable platform, in order to satisfy the needs of the project to the maximum, allowing the activation of the different modules and functions according to the requirements.


Follow-up can also be registered by the same participant through the TrialPal mobile application, where forms and surveys can be configured so that the user reports important information for the study; information that can be viewed from the PFS by users of the sites, either in a general or detailed manner.

PFS, allows the collection of all the data necessary for decision making, allowing the visualizationg of the traceability in changes, guaranteeing the transparency of the information provided.

Its main

characteristics are:

  • Configurable tool

  • Dynamism for the management of visits and follow-up to patients

  • Record of all activities and events of a subject

  • Traceability and auditing of all actions carried out on the platform

  • Use of Trial Pal mobile application to collect data in the first person

  • Download reports and information directly from the platform

If you want to know more about how our systems are validated and comply with 21 CFR Part 11

Do you want to chat and know more about any solution?

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Integration between EDC, eCOA and Site CTMS

Our eCRF, TrialPal & PFS or Trial 360 combined 

The combination of three of our best solutions resulted in an easy to use platform for all the needs of your site.

Monitoring of study participants and the study in general, minimizing processes, reducing costs, keep a tracking on eDiaries and registers, further to monitoring the information in a clinical study; all in one integration.

Integration Model

Below you will find an integration example. Our solutions include an easy to configure API that extracts data from our ePRO or eCOA to Site CTMS and along with or CRF Importer is then transferred to our proprietary eCRF or to 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 reviews and compares data between systems so the site can be confident that all data was transferred successfully and that data integrity has been met.


  1. Integrations take 2-3 weeks (approx) depending on study forms (# variables, visits, e-dairy days).

  2. Testing and validation takes 1 week (approx), to ensure integration works flawlessly.

  3. Rave dedicated user needed to authenticate transactions via RWS.

All digital, less time, save $

No more loss of information, no more hiring of digitization services, and no more human errors. Get savings. Allow remote access to CRAs. Be efficient

Customized stats

Real-Time with ablility to export to excel, containing customized stats and data

Get close to your patient or subject

Receive immediate notifications of any patient report, act quickly, gather insights and respond to study objectives. Use the end-user preferred communication method such as secure chat, schedule visits, and easily set up a new study within a couple of hours according to study protocol.


All your data completely safe and systems 21 CRF Part 11 Compliant

Click on each solution

If you want to know more about it


If you want to know more about how our systems are validated and comply with 21 CRF Part 11

Want to get any of the solutions?

Schedule a meeting with us


Study Cases

Grateful customers

At Integra IT we care about the satisfaction of our clients and the good performance of each of our solutions, always providing clients with the best support and listening to each request they may have.

Here are some of our study cases:



Our solutions helped CEVAXIN to improve on its efficiency and management of data in every one of its clinical studies, helping it to make less mistakes and gather all the information digitally and securely.

University of Mainz

The university was in charge of one of the studies for Covid 19. Using our Winning Formula (PFS II and TrialPal), it was able to organize everything regarding the studies during pandemic times and to manage all the study results and data.

"The TrialPal Mobile App made it possible for 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 Success

What do our customers say