Senior Program Manager, Medicines Licensing & Pharmacovigilance
Danish Medicines Agency
Ditte Zerlang Andersen joined the Danish Medicines Agency (DKMA) in 2015 and have for the past decade led strategic projects in our national and EU regulatory landscape facilitating cross-functional collaboration across Member States to establish policies and optimize procedures. She is currently program manager of the ‘COMBINE’ programme that seeks to make the European Union attractive for conduct of combined studies, envisioning a clear and smoothly functioning regulatory environment for combined studies through broad involvement of all impacted stakeholders. She previously led work to clarify guidance on complex and decentralised trials and prior joining DKMA, worked 5 years in the pharmaceutical industry and have a PhD in neuroscience.
Clinical Investigations for Combined Use Systems
Thursday, November 13, 2025
11:25 AM - 12:25 PM East Coast USA Time