The Online-Seminar will take place in 8 months, on 06-27-2024 from 13:30 – 17:30 .

Risk Management for Medical Devices II

Which regulatory requirements must be adhered to minimize risk and which implementation is requested by the MDR? Our auditor and expert, Dr. Hogh-Janovsky, will explain the relevant requirements of the MDR in more detail with you in Part II.

Target group and previous knowledge

The participants should be able to fundamentally transfer the normative requirements and their elements to the specific needs of their company. Basic knowledge of the risk management standard ISO 14971 is required.

Contents

  • Medical Device Regulation (MDR)
  • Risk-based approach
  • Risk management standard EN ISO 14971
  • General obligations of manufacturers according to MDR
  • Risks in distribution chains

Discounts

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.

Notes

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.

Price per participant

450.00 Euro (plus value added tax)