Programme

2015, March

Last May, the European (EU) Council published its position on the draft regulations for Medical Devices and IVD. Despite not being the final version, the position of the EU Council provides some insight and a better understanding of the regulation to be discussed by the “Constitutional Triangle” composed of the EU Commission, Parliament and Council. The final adoption of the new regulation is expected to significantly revamp the current EU Directives regulating Medical devices (MD) and In vitro Diagnostics (IVD).

In this webinar, we will analyze the positions of the three main actors (EU Commission / Parliament / Council), focusing on the potential changes affecting the classification of MD and IVD devices.

The topics covered in this webinar include:

  • The state of the EU regulations and the processes it entails
  • The evolution of the EU regulations
  • Possible classification changes and the corresponding pathway for CE Marking
  • Potential impacts for MD and IVD manufacturers

Experts

Anne LE ROUZO Sr Lead Auditor ISO 13485, ISO 9001, CMDR, MDD, AO regulations

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