Medical and Regulatory Affairs

About

The Medical and Regulatory Affairs team at Novo Nordisk oversees the development, dissemination, and enforcement of medical guidelines and regulatory compliance within the company’s global operations. This team ensures that all pharmaceutical products, particularly those aimed at diabetes, obesity, rare diseases, and other chronic conditions, meet rigorous safety and efficacy standards while navigating the complex landscape of international medical regulations. They work collaboratively to facilitate clinical trials, secure regulatory approvals, manage patient access programs, and uphold corporate compliance and privacy standards.


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