Amko Groeneveld
Project Manager; Coordinator International Regulatory Affairs, novineon CRO GmbG
Formal Education. B.Sc. Medizintechnik; M.Sc. Medizintechnik - Regulatory Affairs+5 years of experience in working medical device regulatory affairs at novineon CRO, with an emphasis on clinical data, clinical evaluation, MDR transition, and FDA submissions.
Events Amko Groeneveld has spoken at
- MEDICA 2026 16 November 2026 – 19 November 2026