Sensius appoints David Restuccia as Regulatory Affairs & Quality Assurance Head

Sensius appoints David Restuccia as Regulatory Affairs & Quality Assurance Head

David has worked as a Regulatory, Clinical, and Scientific Affairs Consultant for medical device and pharmaceutical manufacturers since 2018. His primary focus is ensuring compliance and managing the registration of medical devices under the EU Medical Device Regulation (MDR). David joins the Sensius team to provide regulatory and quality support.

His experience spans a wide range of device types - including active, diagnostic, invasive, implantable, and software-based technologies - across therapeutic areas such as oncology, ENT, neurology, orthopaedics, dentistry, and surgery.

Before moving into Regulatory and Clinical Affairs, David studied Medical Science at the University of Sydney, Australia, and was awarded a PhD in Biochemistry from the University of Basel, Switzerland for his doctoral research, conducted at the Friedrich Miescher Institute for Biomedical Research entitled “Protein Kinase B: The Beta Version – Elucidating Novel Contributions of Protein Kinase B Beta (PKBβ/Akt2) to Endocrine Metabolism, PCOS, and Cancer.”