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    Sonia Disha

    Sonia Disha

    Regulatory expert, Scilife

    with 8+ years of experience in the medical field, Sonia is well-versed in FDA, EU MDR, and international standards, focusing on quality and excellence. She employs her clinical expertise in helping medical brands globally and has successfully enhanced global client reach through strategic and cross-functional collaboration. Passionate about regulatory affairs and healthcare innovation, she is committed to driving compliance excellence and advancing industry standards.

    More articles from Sonia Disha

    Mastering Total Quality Management in your organization

    Quality in life sciences is more imperative than ever. Organizations today are under constant pressure to innovate and meet market demands while simultaneously improving efficiency, maintaining regulatory standards, and minimizing risk.

    Design History File (DHF): Everything you need to know + Checklist

    Unlike futuristic tech and devices, the medical device industry prefers simple designs. A simple to use, easy-to-use interface is crucial in devices providing life-saving treatment. However, that does not mean that designs do not take priority in med...

    Good Pharmacovigilance Practices (GVP) explained and how to do it righ...

    What is pharmacovigilance? Before we dive into what Good Pharmacovigilance Practices (GVP) are, it’s important to first explain the term pharmacovigilance.

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