
When the cost of getting compliance wrong can include fines, regulatory action, legal liability, and reputational harm, completion rates alone aren't enough. Compliance, HR, and L&D leaders need evidence that their programmes are changing behaviour and reducing risk, yet many organisations still rely on outdated tick-box training or inadequately governed AI-generated content.
That's why more than 1,400 organisations trust Skillcast. For over 25 years, we've combined compliance expertise, AI-powered technology, and rigorous human oversight to help organisations:
- Centralise compliance learning, policies, disclosures, and registers.
- Increase engagement through personalised learning pathways.
- Strengthen governance with policy attestations and disclosure management.
- Maintain audit-ready records and compliance reporting.
- Provide instant AI-powered guidance grounded in trusted business content.
- Seamlessly edit our expert courses using AI without sacrificing oversight.
- Deploy solutions that are off-the-shelf, configurable, or fully bespoke.
The result is reduced risk, stronger compliance cultures, improved employee decision-making, and confidence that your organisation is meeting its regulatory obligations with a partner that understands what's at stake.
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Code-Cube.io is an advanced marketing observability platform built to safeguard the accuracy of dataLayers, tags, and conversion tracking across digital environments. It continuously monitors tracking systems to identify issues such as broken tags, missing events, or delayed data collection in real time. By delivering instant alerts, the platform allows teams to resolve problems quickly before they negatively impact campaign performance or analytics reporting. Its automated quality assurance capabilities eliminate the need for manual checks, reducing operational overhead and increasing efficiency. Tools like Tag Monitor provide detailed visibility into tag execution across both client-side and server-side setups, ensuring nothing goes unnoticed. DataLayer Guard enhances this by validating every event, parameter, and value to maintain clean and consistent data streams. The platform supports multi-domain tracking, making it ideal for businesses managing complex digital infrastructures. It helps prevent wasted advertising budgets by ensuring marketing algorithms receive accurate signals for optimization. Code-Cube.io also improves collaboration across teams by offering clear insights into root causes of tracking issues. With enterprise-grade reliability and GDPR compliance, it meets the needs of global organizations. The platform is trusted by leading brands to maintain data integrity at scale. Overall, Code-Cube.io enables businesses to operate with confidence by turning unreliable tracking into a dependable foundation for growth.
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Medrio
Since 2005, Medrio's Electronic Data Capture (EDC) platform and its complementary eClinical solutions like ePRO, RTSM, eConsent, and Direct Data Capture (DDC) have gained the trust of leading pharmaceutical, biotech, CRO, animal health, medical device, and diagnostic organizations.
Our reputation is built on providing user-friendly solutions that enhance the efficiency and simplicity of clinical trials across all phases, sizes, and complexities. Users of Medrio can create their databases in an average of 2.8 weeks without needing any programming skills and can easily implement mid-study modifications with just a few clicks.
With options ranging from add-on features to comprehensive service packages, Medrio delivers adaptable, modular solutions tailored to meet the precise needs of our clients, ensuring they receive only the services they require. Our cutting-edge software, combined with extensive training and support resources, has resulted in a remarkable 98% customer satisfaction rating, demonstrating our commitment to excellence in the clinical trial landscape. We continuously strive to innovate and improve our offerings to keep pace with the evolving needs of our users.
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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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