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.
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...
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