Janine Treter

Janine Treter, PhD, is a Regulatory Affairs Specialist at Philips, where they focus on the design, development, and regulatory strategy for Software as a Medical Device (SaMD) registration worldwide. Janine earned a degree in Pharmacy in 2008 and a PhD in Pharmaceutical Sciences in 2013. With nearly a decade of experience in medical device regulatory affairs, they have worked with multiple regulatory bodies including ANVISA, FDA, Health Canada, TGA, and EU MDR. Janine has previously held positions at companies such as Neodent, Angiomed Importação e Exportação Ltda, and Vitalife Produtos Fármaco-Hospitalares, where they contributed to various regulatory processes and compliance efforts.