Regulatory Affairs
- Submission of AMG/CTR studies to regulatory authorities via CTIS (EK, BfArM, PEI) and DMIDS for medical device studies
- Medical Writing Support
- Organizational and location details for the MHH site
Dr. Ute Denkena
mobile: +49 (0) 1761-532-7239
email: Regulatory.zks@mh-hannover.de