Regulation (EU) 2017/745
Do you need more information about the requirements your company must meet regarding the regulations in force in the sector?
The challenge
Regulation (EU) 2017/745 on medical devices sets out the rules on the placing on the European Union (EU) market, the placing on the market and the putting into service of medical devices for human use and their accessories. Implementation of this regulation improves patient safety by introducing stricter conformity assessment procedures (to ensure that unsafe or non-compliant equipment does not reach the market) and post-market monitoring.
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