OrangeHRM Advanced
Elevate your HR strategy with OrangeHRM, a world-class HRMS designed to help you and your team shine as organizational heroes. Whether you are looking to automate routine processes or manage the end-to-end employee lifecycle, our platform provides the comprehensive tools necessary to drive success. Join the thousands of businesses worldwide currently transforming their operations with OrangeHRM.
Built to scale with your ambition, our software supports everyone from emerging startups to multinational corporations. We simplify complex workflows through powerful management capabilities, including:
-HR Administration
-Employee Management
-Reporting & Analytics
-Mobile App
-Recruitment
-Onboarding
-Request Desk
-Leave Management
-Time and Attendance
-Roster
-Performance Management
-Career Development
-Training
-Surveys
-Employee Voice
-Discipline
With flexible cloud and on-premise hosting options, OrangeHRM makes HR automation simple, secure, and effortlessly efficient.
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SiteKiosk
SiteKiosk Online offers a comprehensive and secure software solution for kiosks and digital signage that is compatible with both Windows and Android platforms. Their user-friendly and scalable application, SiteKiosk, safeguards the browser and operating system from unauthorized changes while ensuring continuous maintenance-free functionality around the clock. This service not only enhances security but also simplifies the management of digital displays.
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Folio3 Clinical Trial Management
Folio3 Digital Health presents a comprehensive Clinical Trial Management Software (CTMS) designed as a web-based solution to significantly improve the overall effectiveness of the clinical trial lifecycle for pharmaceutical companies, contract research organizations (CROs), and research institutions. This innovative platform integrates multiple trial operations, streamlining processes from planning and site management to data collection and reporting while ensuring compliance with international standards such as FDA 21 CFR Part 11, GxP, and HIPAA regulations. With an emphasis on user-friendly interface designs and real-time dashboards, the software is adept at managing clinical trials of all sizes efficiently.
Included in the system are specialized modules for initiating studies, which allow users to define protocols, establish timelines, and create budgets through customizable templates that meet their specific requirements. Additionally, the site management capabilities facilitate the tracking of investigator credentials, contracts, and financial transactions, alongside patient recruitment features that simplify the screening process, monitor enrollment, and organize visit schedules, complete with automated reminders to boost participant involvement. The platform's adaptable nature ensures its relevance for a variety of stakeholders in clinical research, ultimately fostering a more cohesive and effective trial management experience, which is essential for advancing medical knowledge and improving patient outcomes. Furthermore, its robust analytics tools provide valuable insights that can enhance decision-making throughout the trial process.
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SimpleTrials
SimpleTrials is a subscription-based, on-demand Clinical Trial Management System (CTMS) specifically designed for sponsors, Contract Research Organizations (CROs), and research facilities. It offers a comprehensive suite of tools that streamline the planning, management, and oversight of clinical study portfolios, including features for site initiation, subject monitoring, and document management via an integrated electronic Trial Master File (eTMF). Users can take advantage of real-time analytics for their studies, detailed calendars, customizable fields and trackers, on-demand reporting, planning milestones, and the management of site contracts and payments, along with electronic documentation of visits. The platform is constructed to adhere to 21 CFR Part 11 compliance standards, providing a secure and validated environment for the handling of clinical trial data. Additionally, users can customize their tracking views, seamlessly connect with various Electronic Data Capture (EDC) systems, and utilize pre-built templates for consistent document management. By fostering enhanced collaboration among all stakeholders, the system supports more effective communication throughout the entirety of the trial process, ultimately leading to improved outcomes and efficiency in clinical research.
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