Aftagerpanel for Master of Industrial Drug Development og Master of Medicines Regulatory Affairs

 

  • Master of Industrial Drug Development
  • Master of Medicines Regulatory Affairs

 

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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