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Florian Tolkmitt

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Development: -Broad experience in development of medical devices, especially single use devices and implants. (example: -Experience with patent research and application for various medical devices. -Cooperation with a broad range of medical device manufacturers in Germany. Regulatory Affairs: -Expert for clinical affairs with specialty in clinical evaluation of medical devices. -Expert for technical documentation with specialty in Summary technical documentation (STED). -Expert for demarcation of medical devices and medicinal products. -Specialist for quality managment and risk management for medical device manufacturers. Goals: -Building up the international branch of our regulatory compliance services, especially US and latin american buisiness.
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University of Applied Sciences Wilhelmshaven
Dipl.-Ing. (FH)
1999 To 2003

Brookville High School
High School Diploma
1995 To 1996

Christian-Dietrich Grabbe Gymnasium
Abitur (A-levels)
1994 To 1998

Job History

Head of Regulatory Affairs
June 2012 - present

Functional Head
January 2008 - March 2012

Project Engineer for Regulatory Compliance
January 2007 - January 2008

Development Engineer for Medical Devices
January 2003 - January 2007

Regional Areas of interest

  • Global