Results

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, a multi-site, multi-study, multi-country organization with a recruitment module, Project and Study set-up plus scheduling, Electronic Medical Record, and Laboratory module. These four modules constitute the basis of a Site compliant with the best practices guidelines.

Sites can grow quickly after 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.

VRT main objective is to have a control in the cloud that in real time manages the vaccination plan of the entire population of the country. Reduce information availability and consolidation times through the interconnection of nurses, statisticians, staff, and the centralization of all information on vaccinated people and their respective cards.

Time measurement system and Clinical Research Registry in countries, local authorities or guilds.
It is a web application that allows you to have an updated and permanent record of all the clinical studies carried out in the country from the initial evaluation to its completion.

The STS is a web-based system designed so CROs (Contract Research Organizations) can optimize, record, and follow up visits to research sites with high-quality standards. Our STS tool allows a complete registration and report of the CRAs (Clinical Research Associates) visits to each research site during one or multiple clinical trial conductions with easier operational management for the Project Manager (PM).
Within the STS we have electronic signatures for monitors and Project Managers to certify that all processes are carried out according to best practices.

The best cost-benefit eCRF/Electronic Data Capture (EDC) easy-to-set web solution in the market. Combined with our TriaPal ePRO/eCOA mobile solutions and Data Management capabilities, our services outstand in deliverables timing and quality.
We foster high levels of efficiency, ensuring transparency, data integrity, and quality of your data.

PFS is a web system intuitive and easy-to-use tool for monitoring the clinical trial participants and the whole trial. Therefore it is the application where all the information collected by our TrialPal is centralized. A specialized software based on highly reliable and available platforms that guarantees an excellent service performance without interruptions, integrating security standards, and guidelines such as CRF Part 11 from the FDA. This system is designed mainly for the Sites and will allow efficient management of subjects and the trial.

We are an Appian, Microsoft, and Google Cloud partner company that provides SAAS Software as a service through information technology and aerospace, transportation, and healthcare consulting employment experts around the world. We integrate intuitive software design for users, create robust and scalable Software through Machine Learning technologies, integrate multiple data sources in a single system, and have advanced technology products and services.

we solve complex problems oriented to processes that guarantee the efficiency and productivity of organizations with technologies in the cloud.

eCOA/ePRO DCT mobile and web application, is a solution that captures information directly from the patient from a cell phone, contains a differentiating factor, generating value by offering solutions for monitoring and defining processes; reports in the form of a dashboard, including the information collected. Alerts and notifications are generated, and a projection helps decision making.

We are the first technology company in the Life Science industry to serve clinical trials and patient programs in Latin America integrating data from patients, sites, CROs, and Sponsors. With global reach and US-based, we have created agile, flexible, and validated-secure solutions that use real-time data from patients to sponsors to improve decision-making, reduce costs and contribute to the world's health and quality of life. 
We offer a solutions suite 100% cloud-based, in compliance with the 21 CFR Part 11 guidelines from the FDA and the GCP (Good Clinical Practices). Our purpose is to make clinical trials' performance more efficient through high-end technology while making them person-centered.

We are a Colombian knowledge company with a presence in the United States, with the primary purpose to support and provide business transformation through advanced technological tools and platforms.
We know that technology is vast and sometimes overwhelming; we want to make it easy and affordable.

We have extensive experience in different lines of business, and we carry out projects and maintain the platforms of strategic allies in the financial and educational sectors.

Our commitment, dedication, quality, and cooperation characterize us. We strongly believe that we must fully align with our allies to provide an efficient and excellent service and far-reaching technological solutions.