Daniel Rubisoier

Regulatory Affairs Specialist, TÜV SÜD, Austria
  • Overall responsibility to assure that all processes at TÜV SÜD implemented by corresponding process owners in line with the regulatory requirements of the MDR.
  • Responsibility for up-to-date compliance to the assigned conformity assessment scheme and applicable standards.
  • Creating awareness for the essentials of the conformity assessment scheme and related changes.
  • More than 10 years of professional experience with medical devices in the field of quality and regulatory under the directives (MDD/AIMDD) and the regulation (MDR) in industry.