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Hours of Operation Closed now

  • Saturday 09:00 AM - 06:00 PM
  • Sunday 09:00 AM - 06:00 PM
  • MondayClosed
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10006 Cross Creek Blvd. Suite 71 10006 Cross Creek Blvd. Suite 71, Tampa, FL 33647


CQ-eu mdr - Introduction

EU MDR (The European Union Medical Device Regulation) is a regulatory framework that applies to all European medical device manufacturers to establish high quality and safety standards for medical devices production.

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  • CQ-eu mdr

    In the modern world, the life sciences sector is going through a period of unprecedented regulatory change affecting organizations involved in pharmaceuticals, medical devices, and in-vitro diagnostics. The European Union Medical Device Regulation (EU MDR), a robust, transparent, predictable and sustainable regulatory framework for medical devices, ensures high standards of quality and safety being produced in or supplied into Europe.

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