Medical Devices – Clinical and Regulatory Affairs
In total about 25 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 10 years international experience as senior expert and consultant in the areas Medical Device R&D, Regulatory Affairs, Clinical Affairs.
Since January 2004 owner and managing director of the PROREGITAS Medical Consulting (service provider with focus on Medical Device Regulatory Affairs, Clinical Research and R&D).
Areas of Expertise:
MD Clinical Evaluations, MD Quality Management, MD Regulatory Affairs