Trial 360
Clinical Trial Management
System (CTMS) + eSource + ERP

Talk with an Expert

Trial 360
Clinical Trial Management System (CTMS) + eSource + ERP

Talk with an Expert

Best combined with:

Clinical Trial Management System (CTMS), Enterprise Resource Planning (ERP), Customer relationship management (CRM) and eSource (EMR)

Trial360 is a web-based 21 CFR Part 11 compliant platform that speeds up processes and improves quality across the clinical trial. Inspired by a site’s network, this modular and user-friendly solution adapts to any site size as well as various studies for the investigational site at the same time.This tool has been used in sites to support multi-study, multi-site and multi-country organizations. Featuring several core modules: Research Projects, Recruitment, Scheduling, eSource: electronic medical record (EMR), Laboratory, pharmacy, Imaging. This integrated system allows in an organized and stress free manner investigational sites to comply with clinical practice guidelines.


Grow your sites even faster by installing the Enterprise Resource Planning (ERP) modules such as Finance and Billing, Procurement and Inventory, Human Resources, Document Management, eLearning, etc., on an on-demand basis and with a pay-as-you-go model.

Clinical Trial Efficient Process

Easy and fast Protocol setting in a validated, user-friendly, all-in-one web solution:

Quick Project Set Up (By Project)

Recruitment (CRM - Website)

Management (Visits & eSource)

Data Analysis


100% Satisfactory FDA Inspections

Feature One

Quick Project Set Up (By Project)

Feature Two

Recruitment (CRM - Website)

Feature Three

Management (Visits & eSource)

Feature Four

Data Analysis

of Trial 360

  • Build tailored trials, multi-studies, and multi-sites.
  • Reduce study startup timelines by 3 – 4 weeks.
  • Swift, cost-effective conduction of trials.
  • User-friendly software tools with a person-centered approach.
  • Easy-to-use and accessible from any browser, anywhere at any time.
  • Automated workflows.
  • Integrate with your EDC, IRT, and other systems like RAVE.
  • Comprehensive user management according to role and permissions granted.
  • Creation of monitor-type users (allows remote monitoring).
With Trial360, line up your Research Site operations with your goals and exceed results
Trial 360 core modules for clinical trials:

Study Configuration



eSource (EMR)






Cross-Sectional System Features







Real-time collaboration

Comprehensive management of users according to role and permissions granted.

Allows the user to create a Monitor role (when remote monitoring is enabled).

Dismiss paper usage

Download the Trial 360 Specsheet

Early Adopter
Program Terms

Our Trial 360 Early Adopter Program gives a preferred rate of USD 48 per user to start with. It includes the seven characteristics of the initial core system that is enough to conduct a first clinical trial. More as follows:

The initial core system includes:

  1. Recruitment CRM: Record potential participants process up to enrollment and use the personalized website for engaging new candidates.
  2. GCP Compliant Electronic Medical Record 21 CFR Part 11 validated.
  3. Projects Application: the main section where the projects are configured and defined according to the protocol, including groups, visits, domains of the Electronic Medical Record per visit, inclusion/exclusion criteria, scheduling according to the window, etc.
  4. Laboratory management system integrated with the electronic medical record and connected to a local or central Laboratory system – LIS.

A private infrastructure with up to 100GB of storage and 5×8 functional support.

The cost of the program varies according to the size of the site, and the type and amount of training required per user.

Finance, Accounting, Expenses, Procurement, Inventory, Human Resources, Time Sheets, eLearning, Docs, etc., with a cost per application plus implementation services.

NOTE: Prices do not include taxes. Discounts between 10-20% are available when purchasing in bulk.

Explore your clinical trial possibilities

Luz H Barreto

Luz H Barreto

Medical Director

Click the calendar to schedule a meeting

Why Integra IT

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

Want to know more about our Trial 360 Clinical Trial Management?

Schedule a meeting with us!

Trial360 Medical Record