Daniela Levy, Advocate Founder of Sterling Medical Registration Regulatory & Quality Consultant with 27 years experience in the Medical Device industry, specializing in Global Product Registration and Quality System Implementation. Former VP of Regulatory & Quality Affairs at Alpha Bio Tec Ltd, where she led the due diligence and project support during the company’s acquisition by Nobel Biocare AG. Known for her integrity, professionalism, and commitment to excellence.
Read MoreResponsible for overseeing regulatory compliance across all client engagements. Ensures that medical device documentation, processes, and submissions meet international standards and regulatory requirements.
Responsible for overseeing quality assurance across all client engagements. Ensures that medical device and quality assurance are up to date and meet international standards and regulatory requirements.