Das Online-Seminar findet in 4 Monaten, am 26.06.2024 von 13:30 – 17:30 Uhr statt.

Risk Management for Medical Devices I

Risk management as a central demand for medical devices has to be established for all activities of the life cycle of medical devices- As a medical device manufacturer, you are obliged to implement and document a risk management process and related procedures. Our auditor and expert, Dr. Hogh-Janovsky, will demonstrate the normative terms and requirements of the risk management standard EN ISO 14971 in Part I. The required risk management process in companies is systematically examined using practical examples.

Zielgruppe und Vorkenntnisse

For employees who are involved in the risk management process and in the creation of technical documentation. The seminar provides basic knowledge with a further outlook and is suitable as an introduction to the topic.

Inhalte

  • Risk management standard EN ISO 14971
  • Terms and structure
  • Responsibilities in the company
  • Required process steps and their documentation

Ermäßigungen

Participant discount: From the 2nd participant you will receive a discount of 15% on the net price.

Customer discount: mdc customers receive a 10% discount on the net price.

Hinweise

Participant and customer discounts cannot be combined!

Please note that the registration fee and the associated participation only applies to one person. If several people take part in the seminar (remotely) even though only one person has registered, we reserve the right to exclude them from the seminar.

Preis pro Teilnehmer

450.00 Euro (zzgl. ges. MwSt)