Experience:
In total about 30 years international management working experience in the pharmaceutical and medical device industry:
About 11 years industry experience in the management of pre-clinical and clinical research and development projects in various indications.
About 16 years international experience as senior expert and consultant in the areas Medical Device R&D, Clinical and Regulatory Affairs.
Since January 2004 owner and managing director of the PROREGITAS Medical Consulting (service provider with focus on Medical Device Clinical Affairs and Regulatory Affairs).
Since 2009 external lecturer at the TUEV Rheinland Academy.
Areas of Expertise:
Medical Device Clinical Investigations, PMCF, Clinical Evaluations, Regulatory Compliance (acc. MDR, MDD)
