Kamilla Nanda Kampmark

Kamilla Nanda Kampmark is a seasoned professional with extensive experience in regulatory affairs and clinical document management. Currently serving as a CTA Global Regulatory Affairs Manager and Clinical Document Manager at Ferring Pharmaceuticals since February 2019, Kamilla has a strong background in managing high-quality regulatory submissions, including Clinical Trial Applications and Marketing Authorization Applications. Prior roles include Regulatory Affairs Associate at Novo Nordisk, where responsibilities encompassed regulatory document management and pharmacovigilance support, and various administrative positions in healthcare settings. Educational qualifications include degrees in Graphic Design and Oral Health from Griffith University and The University of Queensland, as well as studies in Creative Arts and Medicine from James Cook University.