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Public Health

The following new legislation is applicable within the EU

The EU has revised the legal framework of the current 3 directives to reflect progress over the last 20 years. Adopted in May 2017, the new rules will fully apply after the transitional periods provided for in the regulations.

The new regulations contain a series of extremely important improvements to modernise the current system. Among them are

  • stricter previous control for high-risk devices via a new pre-market scrutiny mechanism with the involvement of a pool of experts at EU level
  • reinforcement of the criteria for designation and processes for oversight of notified bodies
  • inclusion of certain aesthetic devices that present the same characteristics and risk profile as analogous medical devices under the scope of the regulations
  • a new risk classification system for in vitro diagnostic medical devices in line with international guidance
  • improved transparency through a comprehensive EU database on medical devices and a device traceability system based on a unique device identification
  • introduction of an ‘implant card’ for patients containing information about implanted medical devices
  • reinforcement of the rules on clinical evidence, including an EU-wide coordinated procedure for authorising multi-centre clinical investigations
  • strengthening of post-market surveillance requirements for manufacturers
  • improved coordination mechanisms between EU countries in the fields of vigilance and market surveillance

See the new rules to ensure safety of medical devices.

All actors involved with medical devices, from their manufacture to their use, have to comply with the new regulations by May 2021 (May 2022 for in vitro diagnostic medical devices).

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