Director of Neurointerventional Regulatory Affairs @ MCRA
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Robert Herrmann Location
Washington, DC, US
Robert Herrmann Work
2021 -
now Director of Neurointerventional Regulatory Affairs @
2016 -
2021 Team Lead Neurointerventional Devices @ FDA CDRH
2015 -
2016 Lead Reviewer Neurointerventional Devices @ FDA CDRH
2008 -
2015 Vice President Engineering @ eVasc Medical Systems
2006 -
2008 Engineering Manager @
2000 -
2006 Principal Scientist, Sr. Research Scientist, Research Scientist @
1998 -
1999 Post-Doctoral Researcher @
1996 -
1998 Post-Doc and Consultant @ Department of Cardiology, Klinikum rechts der Isar, Munich, Germany
1988 -
1990 Project Engineer @ Canon Virginia
Robert Herrmann Education
Duke University 1990
-
1996
University of Virginia 1982
-
1986
Robert Herrmann Skills
Quality System Compliance
Medical Device Clinical
Design Control
Engineering Management
ISO 14971
Verification And Validation V&V
GMP
Biomaterials
Biomedical Engineering
Biotechnology
Regulatory Affairs
Team Management
Validation
Biocompatibility
Medical Devices
Combination Products
Engineering
Quality System
Research And Development R&D
Product Innovation
Budget Management
Program Management
V&V
Spring
Clinical Development
Design of Experiments
In Vitro
U.S. Food And Drug Administration Fda
Silver
CE marking
Medical Device R&D
Spring Framework
Toner
Project Management
Biomedical Engineer
CAPA
FDA
R&D
Commercialization
ISO 13485
Research and Development
u.s. Food and Drug Administration
Verification and Validation
Robert Herrmann Summary
Robert Herrmann, based in Washington, DC, US, is currently a Director of Neurointerventional Regulatory Affairs at MCRA. Robert Herrmann brings experience from previous roles at FDA CDRH, eVasc Medical Systems and Angiotech Pharmaceuticals. Robert Herrmann holds a 1990 - 1996 Duke University. With a robust skill set that includes Quality System Compliance, Medical Device Clinical, Design Control, Engineering Management, ISO 14971 and more. Robert Herrmann has 4 emails on RocketReach.
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