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    Rebecca Beausang

    Rebecca Beausang

    Regulatory Affairs Specialist, Scilife

    Rebecca has over seven years of experience in medical device and other regulated industries. Alongside her expertise in FDA submissions, EU MDR compliance, and ISO 13485 QMS implementation, Rebecca is skilled in creating clear and impactful regulatory content. From technical documentation to compliance blogs, she excels in translating complex topics into engaging, actionable insights. Her passion lies in using compliance as a strategic tool to drive innovation and trust in regulated markets.

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    Why pharma AI pilots fail: A governance perspective

    TL;DR Most pharma AI pilots stall because they were designed to prove that a model works, rather than whether it can operate inside a regulated production environment. Common barriers include fragmented data, unclear ownership, late-stage validation ...

    ISO/IEC 42001 explained: the AI management system standard for life sc...

    Quick answer: What is ISO/IEC 42001? ISO/IEC 42001 is the first international standard for establishing and continually improving an AI management system. For life sciences organizations, it provides a structured way to govern AI risks, responsibilit...

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