I'm passionate about developing medicines that will help patients through unlocking both regulatory and access hurdles and striving to make a difference in connecting and improving healthcare systems.Experienced VP of Regulatory Affairs working in the biotechnology industry. Skilled in Biotechnology, Regulatory Requirements, European Medicines Agency (EMA), Life Sciences, and Drug Development. Strong legal professional with a Master’s Degree in Regulatory Affairs from University of Wales, Cardiff.
Listed skills include Regulatory Affairs, Pharmaceutical Industry, Regulatory Submissions, Biotechnology, and 12 others.