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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CareLineLive is an all-in-one, cloud-based homecare management platform trusted by over 700 home care agencies and domiciliary care providers across the UK and Australia.
The platform covers rostering, scheduling, care planning, care monitoring (ECM), eMAR, payroll, invoicing and the Care Circle portal for friends and family.
Subscription includes CQC (Care Quality Commission) and CIW (Care Inspectorate Wales) compliance tool MOA Benchmarking to deliver a solution combining both homecare management and compliance.
Customers find the comprehensive functionality easy to use because of the intuitive user interface and enjoy excellent day-to-day support which is recognised by CareLineLive’s high rating on Trustpilot.
CareLineLive is an NHS England Assured Supplier for Digital Social Care Records (DSCR). CareLineLive is accredited to ISO 27001 (Information Security), ISO 9001 (Quality Management), and Cyber Essentials Plus. In addition to being hosted on secure AWS servers with data stored in the UK (or Australia for customers there) for data sovereignty.
Founded in 2014, CareLineLive is led by Managing Director Josh Hough and is headquartered in West Sussex with offices in London and Melbourne. CareLineLive is part of MAS Technicae Group and received majority investment from technology-focused investment firm Accel-KKR in June 2025. Sister companies under the same group include compliance specialist MOA and Australian aged care software provider Health Metrics.
CareLineLive includes:
Electronic Medication Administration Records (eMAR) for medication management
Care rostering software with AI-assisted scheduling
Carer Companion mobile app for Android & iOS
Care Circle Portal for family member access
GP Connect integration for NHS patient records
Payroll and invoicing automation
CQC compliance tools for UK care providers
Fully managed handsets with remote wipe
MOA Benchmarking's audit tool for CQC/CIW compliance
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Castor EDC
Castor is an innovative clinical trial platform designed to simplify data management through electronic data capture (EDC), eConsent, and patient-reported outcomes (ePRO). Its flexible and user-friendly interface allows researchers to collect, manage, and analyze clinical data efficiently across multiple sites and remote patients. Castor’s tools are specifically designed to support decentralized clinical trials (DCTs), enabling real-time data monitoring, remote recruitment, and seamless patient engagement. The platform ensures full regulatory compliance, including HIPAA, GDPR, and 21 CFR Part 11, and is certified for ISO standards. With more than 50,000 global users, Castor continues to improve the speed and quality of clinical trials through integrated, scalable solutions that reduce administrative burdens and accelerate research.
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Cenduit IRT
The complexity of Modern Interactive Response Technology (IRT) systems is on the rise. The importance of customizable and adaptable IRT solutions is paramount, as these systems are crucial for gathering vital information such as recruitment statistics, clinical trial dropout rates, and patient participation. Choosing a user-friendly, mobile-optimized, and comprehensive platform is essential, built on a foundation of quality, flexibility, and expertise. It is essential to engage with a partner that possesses deep therapeutic insights relevant to today’s risk-based eClinical environment. By integrating state-of-the-art technology with specialized expertise and a commitment to outstanding service, we significantly improve clinical trials, ultimately leading to better patient outcomes. Our profound knowledge of clinical workflows and supply chain intricacies drives innovation, empowering clients with enhanced control over their Randomization and Trial Supply Management (RTSM) processes. Our revolutionary tools not only boost quality assurance but also substantially increase site efficiency and patient adherence. Additionally, our versatile IRT platform is designed to accommodate a diverse range of studies and can achieve complete validation and deployment within just 30 days, thereby optimizing clinical trial procedures. This rapid rollout facilitates quicker data acquisition and contributes to a more streamlined overall trial management experience, ultimately paving the way for more effective clinical research outcomes.
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