Tamara Petetta is a Regulatory Affairs Specialist at Aidence, with a focus on regulatory guidance for product registration and compliance for medical devices. With extensive expertise in medical device certification, Tamara ensures adherence to European regulations and US legislation, and is skilled in creating and maintaining technical dossiers and conducting risk management. Prior experience includes roles as a Medical Devices Consultant at ProPharma Group, R&D Project Manager at Serrix Consumer Health, and R&D Specialist II at AkzoNobel Decorative Coatings. Tamara has a strong foundation in research and development from positions at Syngenta and ASSM spa, and completed an internship at Utrecht University focusing on biocompatible polymers. Tamara holds a Master Degree in Chemistry and Pharmaceutical Technologies from the University of Camerino.
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