Daniela Gramaglia is the Associate Director of Medical Device Safety at Bayer, where they assume responsibility for all medical device and combination product safety-related matters. Previously, they served as the Medical Device Vigilance Manager at Chiesi Group, providing medical device safety expertise and collaborating on compliance activities. Daniela has extensive experience in design control, quality assurance, and regulatory compliance, having held various roles in R&D and project management across several organizations. They hold a degree in Pharmaceutical Chemistry and Technology from Università degli Studi di Pavia.
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