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      CASPER E. ULDRIKS


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      Cyber Security Planning for Medical Devices

      MD1556
      CASPER E. ULDRIKS

      Duration: 60 Minutes

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      Training Requirements under FDA’s Quality System Regulation

      FDB1557
      CASPER E. ULDRIKS

      Duration: 60 Minutes

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      Clinical Trials for The Intended Use of Software as a Medical Device

      MD1975
      CASPER E. ULDRIKS

      Duration: 60 Minutes

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      Managing the FDA form “483”: Inspection Observations

      FDB1976
      CASPER E. ULDRIKS

      Duration: 60 Minutes

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      Medical Device Software User Guide – Recovery Steps for Ransom Attacks

      MD1978
      CASPER E. ULDRIKS

      Duration: 60 Minutes

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      FDA Regulation of Mobile Apps – Sure You are Fully Covered?

      FDB2170
      CASPER E. ULDRIKS

      Duration: 60 Minutes

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      Recording
        

      Trimming Back the Burden of FDA’s Software Regulation

      MD2174
      CASPER E. ULDRIKS

      Duration: 60 Minutes

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      Recording
        

      Avoid Reporting Cybersecurity Updates and Patches to the FDA

      MD1977
      CASPER E. ULDRIKS

      Duration: 60 Minutes

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      Recording
        

      EU Medical Devices Regulation – CE Mark Expiration and the EU Refusal of Your Exports

      MD2175
      CASPER E. ULDRIKS

      Duration: 60 Minutes

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