GMED North America, Inc.
GMED North America, Inc.
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The Clinical Evaluation Report (CER) requirements under the EU MDR 2017/745
Tue, Apr 9, 9:00 AM EDT
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Post Market Surveillance & Vigilance: New Requirements under the EUMDR/IVDR
Thu, Apr 4, 10:00 AM EDT
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Technical Documentation per Medical Devices Regulation (EU) 2017/745
Tue, Mar 5, 10:00 AM EST
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BUNDLE: (EU) MDR 2017/745 and Technical Documentation per (EU) MDR 2017/745
Tue, Jan 30, 10:00 AM EST
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European Medical Devices Regulation (EU) 2017/745
Tue, Jan 30, 10:00 AM EST
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Medical Device Single Audit Program (MDSAP) for Manufacturers
Mon, Jan 22, 9:30 AM EST
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Post Market Surveillance & Vigilance: New Requirements under the EUMDR/IVDR
Wed, Nov 1, 12:00 PM EDT
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The Clinical Evaluation Requirements (CER) under the EU MDR 2017/745
Mon, Oct 30, 10:00 AM EDT
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European Medical Devices Regulation (EU) 2017/745
Wed, Sep 27, 10:00 AM EDT
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