GMED North America, Inc.

 

 

 

 

 

Upcoming (1)

Risk Management Applied to Medical Devices (ISO 14971:2019) primary image

Risk Management Applied to Medical Devices (ISO 14971:2019)

Tue, Sep 24 • 10:00 AM EDT

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Risk Management Applied to Medical Devices (ISO 14971:2019) primary image

Risk Management Applied to Medical Devices (ISO 14971:2019)

Tue, Sep 24 • 10:00 AM EDT

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Past (98)

The Clinical Evaluation Report (CER) requirements under the EU MDR 2017/745 primary image

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 primary image

Post Market Surveillance & Vigilance: New Requirements under the EUMDR/IVDR

Thu, Apr 4 • 10:00 AM EDT

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Medical Device Electrical Safety primary image

Medical Device Electrical Safety

Mon, Mar 25 • 10:00 AM EDT

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Technical Documentation per Medical Devices Regulation (EU) 2017/745 primary image

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 primary image

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 primary image

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 primary image

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 primary image

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 primary image

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 primary image

European Medical Devices Regulation (EU) 2017/745

Wed, Sep 27 • 10:00 AM EDT

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Technical Documentation per (EU) Medical Devices Regulation 2017/745 primary image

Technical Documentation per (EU) Medical Devices Regulation 2017/745

Wed, Aug 23 • 10:00 AM EDT

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European in Vitro Diagnostic Devices Regulation (EU) 2017/746 primary image

European in Vitro Diagnostic Devices Regulation (EU) 2017/746

Wed, Jul 26 • 10:00 AM EDT

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The Clinical Evaluation Report (CER) requirements under the EU MDR 2017/745 primary image

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 primary image

Post Market Surveillance & Vigilance: New Requirements under the EUMDR/IVDR

Thu, Apr 4 • 10:00 AM EDT

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Medical Device Electrical Safety primary image

Medical Device Electrical Safety

Mon, Mar 25 • 10:00 AM EDT

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Technical Documentation per Medical Devices Regulation (EU) 2017/745 primary image

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 primary image

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 primary image

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 primary image

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 primary image

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 primary image

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 primary image

European Medical Devices Regulation (EU) 2017/745

Wed, Sep 27 • 10:00 AM EDT

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Technical Documentation per (EU) Medical Devices Regulation 2017/745 primary image

Technical Documentation per (EU) Medical Devices Regulation 2017/745

Wed, Aug 23 • 10:00 AM EDT

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European in Vitro Diagnostic Devices Regulation (EU) 2017/746 primary image

European in Vitro Diagnostic Devices Regulation (EU) 2017/746

Wed, Jul 26 • 10:00 AM EDT

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Events

Risk Management Applied to Medical Devices (ISO 14971:2019) primary image

Risk Management Applied to Medical Devices (ISO 14971:2019)

Tue, Sep 24 • 10:00 AM EDT

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Risk Management Applied to Medical Devices (ISO 14971:2019) primary image

Risk Management Applied to Medical Devices (ISO 14971:2019)

Tue, Sep 24 • 10:00 AM EDT

Check ticket price on event

The Clinical Evaluation Report (CER) requirements under the EU MDR 2017/745 primary image

The Clinical Evaluation Report (CER) requirements under the EU MDR 2017/745

Tue, Apr 9 • 9:00 AM EDT

Check ticket price on event

Post Market Surveillance & Vigilance: New Requirements under the EUMDR/IVDR primary image

Post Market Surveillance & Vigilance: New Requirements under the EUMDR/IVDR

Thu, Apr 4 • 10:00 AM EDT

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Medical Device Electrical Safety primary image

Medical Device Electrical Safety

Mon, Mar 25 • 10:00 AM EDT

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Technical Documentation per Medical Devices Regulation (EU) 2017/745 primary image

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 primary image

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 primary image

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 primary image

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 primary image

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 primary image

The Clinical Evaluation Requirements (CER) under the EU MDR 2017/745

Mon, Oct 30 • 10:00 AM EDT

Check ticket price on event

European Medical Devices Regulation (EU) 2017/745 primary image

European Medical Devices Regulation (EU) 2017/745

Wed, Sep 27 • 10:00 AM EDT

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Technical Documentation per (EU) Medical Devices Regulation 2017/745 primary image

Technical Documentation per (EU) Medical Devices Regulation 2017/745

Wed, Aug 23 • 10:00 AM EDT

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European in Vitro Diagnostic Devices Regulation (EU) 2017/746 primary image

European in Vitro Diagnostic Devices Regulation (EU) 2017/746

Wed, Jul 26 • 10:00 AM EDT

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The Clinical Evaluation Report (CER) requirements under the EU MDR 2017/745 primary image

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 primary image

Post Market Surveillance & Vigilance: New Requirements under the EUMDR/IVDR

Thu, Apr 4 • 10:00 AM EDT

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Medical Device Electrical Safety primary image

Medical Device Electrical Safety

Mon, Mar 25 • 10:00 AM EDT

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Technical Documentation per Medical Devices Regulation (EU) 2017/745 primary image

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 primary image

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 primary image

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 primary image

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 primary image

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 primary image

The Clinical Evaluation Requirements (CER) under the EU MDR 2017/745

Mon, Oct 30 • 10:00 AM EDT

Check ticket price on event

European Medical Devices Regulation (EU) 2017/745 primary image

European Medical Devices Regulation (EU) 2017/745

Wed, Sep 27 • 10:00 AM EDT

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Technical Documentation per (EU) Medical Devices Regulation 2017/745 primary image

Technical Documentation per (EU) Medical Devices Regulation 2017/745

Wed, Aug 23 • 10:00 AM EDT

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European in Vitro Diagnostic Devices Regulation (EU) 2017/746 primary image

European in Vitro Diagnostic Devices Regulation (EU) 2017/746

Wed, Jul 26 • 10:00 AM EDT

Check ticket price on event