The Clinical and Regulatory Affairs Team at P+F Products + Features GmbH ensures that all medical cardiology innovations comply with international regulatory standards and achieve market approval. They manage clinical trials, handle data collection, and oversee quality control and vigilance activities to ensure product safety and effectiveness. The team collaborates closely with research and development to navigate regulatory pathways and expedite the availability of cutting-edge medical technology to healthcare providers and patients globally.
Claudia Rieder
Clinical Project Manager
Mark Hermiller
Area Director Clinical Develop...
Milica Andjelovic
Vigilance & Quality Control Ma...
Paul Shelton
Director Clinical Development
Peter Harmacek
Clinical Data Manager
Robert Artman
Area Director Clinical Develop...
Rolf Seemann
Head Of Regulatory Affairs
Vrushali Tembe
Vice President, Global Regulat...