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Regulation 745/2017 on Medical Devices: post market activities and follow up

September 29 @ 10:30 am - 12:30 pm

$215

Regulation 745/2017 on Medical Devices: post market activities and follow up

Duration: 1 hour

Prerequisite: basic knowledge of medical devices
Recipients:
  • Quality Assurance,
  • Regulatory,
  • Top Management of companies that manufacture,
  • Import,
  • Distribute medical devices in Europe and their suppliers

Contents:

Required updates of Technical File over time; methods for post market follow up according to a risk-based approach

Regulation 745/2017 on Medical Devices: post market activities and follow up

Pre-reserve your seat free and withour any charge (no payment required).
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