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VerifiedMedical Equipment Manufacturing

Requalite Gmbh

Requalite provides Regulatory, quality, and Clinical Study services for in vitro diagnostic and medical device compliance in EU. Requalite is located at the heart of Europe, in Munich-Germany. We provide full CRO services for clinical studies as per IVDR/MDR. In addition, we provide Technical and medical writing services to manufacturers of Medical Device and In vitro Diagnostic devices to obtain CE-marking as per EU regulations of MDR (2017/745) and IVDR (2017/746) for entering European market.

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HeadquartersGrafelfing, GermanyEmployees4(11 to 50)Websiterequalite.comLinkedIn profileLinkedIn

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11 to 50 range

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7

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Monthly traffic

organic / mo

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Top roles at Requalite Gmbh

7 distinct titles indexed · top 7 shown.

  • 1clinical study specialist
  • 1founder and managing director
  • 1office manager
  • 1quality management expert
  • 1regulatory affairs manager
  • 1scientific associate at requalite gmbh
  • 1営業担当者

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