
Qualio is a unified quality and compliance platform that helps growing life sciences companies scale faster while staying continuously audit- and inspection-ready. Medical device, digital health, biotech, and pharma teams use Qualio to replace manual processes and disconnected tools with a single source of truth for quality, regulatory readiness, and risk.
With a modern eQMS at the foundation and Compliance Intelligence layered on top, Qualio moves teams beyond point-in-time audits. Automated gap analysis, cross-standard evidence mapping, and real-time readiness dashboards provide confidence that the organization is prepared today—not just when auditors arrive.
Qualio centralizes document control, training, CAPA, change management, supplier quality, and design controls, linking them directly to regulatory requirements and product lifecycle data. Executive-ready views show compliance health by standard, region, and product, turning regulatory readiness into a measurable business capability instead of a black box.
Compliance Intelligence continuously monitors for risk, highlights gaps early, and prioritizes remediation so teams focus effort where it matters most. Pre-validated regulatory frameworks are maintained as requirements evolve, reducing reliance on consultants and avoiding duplicate work as companies expand.
The result is faster market entry, lower compliance cost, reduced risk of findings or recalls, and confident, risk-managed growth.
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The landscape of access and access management has evolved into a more intricate and often frustrating challenge. strongDM reimagines access by focusing on the individuals who require it, resulting in a solution that is not only user-friendly but also maintains rigorous security and compliance standards. This innovative approach is referred to as People-First Access.
Users benefit from quick, straightforward, and traceable access to essential resources, while administrators enjoy enhanced control that reduces the risk of unauthorized and excessive permissions. Additionally, teams in IT, Security, DevOps, and Compliance can effortlessly track activities with detailed audit logs answering critical questions about actions taken, locations, and timings. The system integrates seamlessly and securely across various environments and protocols, complemented by reliable 24/7 customer support to ensure optimal functionality. This comprehensive approach guarantees both efficiency and security in managing access.
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Adherent
Adherent is an agentic AI platform for product compliance, built to help global companies stay ahead of changing regulations and manage compliance across markets. Formerly known as Compliance & Risks, Adherent combines AI automation with human-verified regulatory intelligence to support trusted compliance decision-making. The platform helps teams monitor product compliance, assess regulatory applicability, identify compliance requirements, prioritize business risk, and manage regulations, standards, requirements, and evidence. Its AI agents handle much of the heavy lifting by tracking regulatory changes, mapping requirements to products, extracting obligations, and identifying risks that need attention first. Adherent is designed for regulated enterprises that require explainable insights, auditable outputs, and strong controls rather than generic AI responses. Ari, the platform’s AI product compliance assistant, acts as a digital teammate that helps execute compliance workflows while experts focus on higher-value strategy. The platform supports compliance needs across corporate compliance, sustainability compliance, C2P compliance, regulations management, standards management, requirements management, and evidence management. It also supports industry-specific requirements for apparel, textiles, footwear, automotive, consumer electronics, cosmetics, household appliances, industrial machinery, medical devices, online retailers, marketplaces, power tools, garden machinery, and toys. Adherent’s regulatory database is verified by global compliance specialists, giving teams access to structured intelligence with human oversight. Customer use cases include horizon scanning, market access, regulatory assessments, compliance monitoring, operational insights, risk prioritization, compliance auditing, and capacity management.
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Safexpert
Safexpert, our extensively tested software, is designed for CE marking and conducting risk assessments in accordance with the Machinery Directive, Machinery Regulation, and Low Voltage Directive. This powerful tool includes various modules that assist you and your team in overseeing safety-related projects while adhering to EU directives and standards. It supports professional safety engineering and modern standard management practices. With direct access to comprehensive full-text standards, it enhances the efficiency of your work. The foundational functions of Safexpert revolve around risk assessments, enabling you to create legally mandated evaluations in a systematic, efficient manner that complies with EN ISO 12100. Additionally, the software offers several features aimed at simplifying the risk assessment process for all involved stakeholders, ensuring that compliance is both manageable and straightforward. This commitment to usability makes Safexpert a vital resource for teams focused on safety and regulatory adherence.
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