Quality Days MDR / IVDR 2026

  • Exchange of experience in the conformity assessment process of Medical Devices (MD) and In Vitro Diagnostic Medical Devices (IVD MD).
  • A comprehensive overview of legal regulations and specific requirements that manufacturers, importers and distributors of MD and IVD MD must follow.
  • Current trends and perspectives in the industry, practical experience and examples of solutions to problems that experts in the field encounter.
  • News and upcoming changes in European and national legislation that will fundamentally affect the procedures for placing medical devices on the market.

The conference will provide a space to gain valuable information, discuss and establish new contacts between manufacturers and regulatory authorities, which can help to better cooperate and more effectively manage the challenges posed by the medical device sector.

Registration for Conference QUALITY DAYS MDR / IVDR 2026 – HERE.

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