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.
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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