Dipl.-Ing. Peter Schrutka-Rechtenstamm

Lecturer for "International Market Clearance of Medical Devices" / "Internationale Zulassung von Medizinprodukten"

Advisor and solution provider at all stages of medical device life cycle, for companies of all sizes (start-ups to multinational enterprises): - regulatory and clinical quick check of early product ideas - global regulatory and clinical strategies of new / changed products; - global approval/ registration planning; - production transfers (e.g. for SKD projects); - challenging compliance situations - RACA role in M&A projects

Head of Global Regulatory and Clinical Affairs

Global Head of Regulatory Affairs

responsible for regulatory affairs and risk management of Voluson Ultrasound products

ADIAM life science AG, Erkelenz (Germany), medical device start-up company (artificial heart valve prostheses and vascular grafts). Manager for Quality Management, RA & QA project manager for IT/ERP introduction internal coach for project management Participation in VC raising.

Engineering & consultancy company for process engineering (basic engineering and conceptual design) for pharmaceutical industry. Managing Director / Geschäftsführer with full managing responsibility for the company