Rameez Raja

With over 13 years of diverse experience, I've worked with top multinational companies on a wide range of regulatory projects, from clinical trials to complex post approval submissions. I specialise in Drugs, Medical devices, and In-vitro diagnostic device regulations. My expertise includes developing and executing successful regulatory strategies. Extensive experience with global regulatory requirements, including EU and emerging markets. Strong problem-solving skills and a research-oriented mindset, with a focus on quality and innovation.