Regulatory Affairs

About

The Regulatory Affairs team at ASPHALION ensures compliance of pharmaceutical, biotech, and medical device products with all applicable international regulatory standards. This involves liaison with EU agencies such as EMA and NCAs, guiding clients through drug development, registration, marketing, and post-commercialization phases, and implementing new regulatory standards efficiently. The team is comprised of highly skilled professionals with deep expertise in Life Sciences and a strong focus on quality assurance and business development.