Aftagerpanel for Master of Industrial Drug Development og Master of Medicines Regulatory Affairs
- Master of Industrial Drug Development
- Master of Medicines Regulatory Affairs
Navn | Titel |
Helle Brøndsted | MSc (pharm), PhD, Product Specialist, DGM Denmark A/S |
Troels V. Christensen | MSc (eng.), Senior Product Life Cycle Manager, H. Lundbeck A/S |
Gitte Dyhr | MSc (pharm), Associate Senior Director, Head of Labelling Committee, Regulatory Affairs, H. Lundbeck A/S |
Jan Fleckner | Ph.D., Director, Translational Science, Biomarker Expert, Novo Nordisk A/S |
Annette Byrholt Hansen | MSc (Pharmacy), PhD, Head of Department, Inspection Laboratory and Inspection Division, Danish Medicines Agency |
Jesper Kihl | MSc (Chem. Eng.), Executive Master (coaching and consulting for change), Senior Advisor, Regulatory Affairs, Keiken Aps |
Frank Larsen | MSc (pharmacy), PhD, Chief Specialist, Clinical & Quantitative Pharmacology, H. Lundbeck A/S |
Katarina Jelic Maiboe | MSc (Pharm), PhD, Vice President Regulatory Affairs, HMNC Brain Health |
Morten Munk | BSc Hon (Chem. Eng), Engineering Technology Management (ETM), Director, Alliance Management, FUJIFILM Diosynth Biotechnologies |
Alejandra Mørk | MSc (Pharmacy), PhD, Managing Director, Klifo A/S |
Helle Northeved | DVM, PhD, Senior Vice President, Nonclinical Safety Research, H. Lundbeck A/S |
Jane Møll Pedersen | Vice President RA Biopharm 2, Novo Nordisk A/S |
Morten Just Petersen | MSc (chemistry), Master of Industrial Drug Development, Chief Development Officer, MonTa Biosciences |
Kresten Skak | MSc (Biochemistry); PhD (Immunology), Senior Director, Immunopharmacology, Dragonfly Therapeutics |
Steffen Thirstrup | MD, PhD (pharmacology), Chief Medical Officer, The European Medicines Agency, Amsterdam, Netherlands |