Ms. Anett Gállné Vályi
Division: Development Engineering
Email:gvanett [kukac] oncotherm [pont] org
Ms. Anett Gállné Vályi has more than 10 years of experience in this field. She is responsible to ensure that our processes are executed according to ISO 13485 (Quality management system for medical devices) standard and our products meet the requirements of 93/42/EEC (Medical Device Directive) and CMDR (Canadian Medical Device Regulations). She is the contact person of our Notified Bodies, TÜV Süd Product Service GmbH and TÜV Süd America Inc.