Matrix eIFU (formerly dokspot) solves the time-consuming and costly challenge of managing traditional paper-based instructions. This cloud-based, turnkey solution guarantees real-time, 3-click access to the latest documentation for healthcare professionals and patients, backed by full audit readiness. Built specifically to meet global regulatory requirements (such as EU Regulation 2021/1226), the platform reduces the complexity and risks associated with manual printing, warehousing, and document version controls. It provides a seamless, white-label end-user experience while giving manufacturers transparent control over their globally distributed compliance documentation.
A startup from Germany.
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eIFU Hosting
Secure cloud hosting for electronic Instructions for Use (eIFU) with instant 3-click access for patients and HCPs.
Regulatory Compliance
Fully aligned with EU Regulation 2021/2226 and EU Regulation 2025/1234 to guarantee compliant digital distribution.
Version Control
Strict versioning and revision history control to ensure users always access the current authorized document.
Matrix eIFU is built specifically for medical device and IVD manufacturers to transition from paper to electronic instructions for use. It ensures strict compliance with EU Regulation 2021/2226 and EU Regulation 2025/1234, providing secure, instant 3-click access to the current approved manuals for healthcare professionals and patients globally.
Matrix eIFU (originally developed as dokspot and now part of the Matrix Requirements ecosystem) was created to solve the massive paper waste, high logistical costs, and compliance risks of printing and shipping physical manuals globally. It was built to streamline compliant distribution of safety instructions.
Unlike generic document hosting services, Matrix eIFU offers a highly secure, regulatory-validated cloud repository. It features strict version control, comprehensive audit trails, localized multi-language portals, and absolute compliance with medical device standards, ensuring users never access outdated or unauthorized instructions.
The primary audience includes medical device manufacturers, In Vitro Diagnostic (IVD) creators, regulatory affairs (RA) professionals, quality assurance (QA) managers, and compliance officers who need to distribute product manuals digitally and securely while maintaining continuous audit readiness.
Matrix eIFU is powered by a secure, cloud-native SaaS architecture. It utilizes end-to-end data encryption pipelines, fast global content delivery networks (CDN) for immediate document access, automated multi-language localization systems, and highly structured, audit-ready database logging.
Global medical device manufacturers (MDMs)
In Vitro Diagnostic (IVD) clinical developers
Software as a Medical Device (SaMD) startups
Life science hardware developers and laboratories
European and global medical equipment distributors
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