GMED North America, Inc.

 

 

 

 

 

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

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

Tue, Sep 24, 10:00 AM EDT

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

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

Tue, Sep 24, 10:00 AM EDT

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Alt (98)

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

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

Tue, Apr 9, 9:00 AM EDT

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

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

Thu, Apr 4, 10:00 AM EDT

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Hauptbild für Medical Device Electrical Safety

Medical Device Electrical Safety

Mon, Mar 25, 10:00 AM EDT

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

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

Tue, Mar 5, 10:00 AM EST

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Hauptbild für BUNDLE: (EU) MDR 2017/745 and Technical Documentation per (EU) MDR 2017/745

BUNDLE: (EU) MDR 2017/745 and Technical Documentation per (EU) MDR 2017/745

Tue, Jan 30, 10:00 AM EST

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Hauptbild für European Medical Devices Regulation (EU) 2017/745

European Medical Devices Regulation (EU) 2017/745

Tue, Jan 30, 10:00 AM EST

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Hauptbild für Medical Device Single Audit Program (MDSAP) for Manufacturers

Medical Device Single Audit Program (MDSAP) for Manufacturers

Mon, Jan 22, 9:30 AM EST

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

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

Wed, Nov 1, 12:00 PM EDT

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

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

Mon, Oct 30, 10:00 AM EDT

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Hauptbild für European Medical Devices Regulation (EU) 2017/745

European Medical Devices Regulation (EU) 2017/745

Wed, Sep 27, 10:00 AM EDT

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

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

Wed, Aug 23, 10:00 AM EDT

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

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

Wed, Jul 26, 10:00 AM EDT

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

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

Tue, Apr 9, 9:00 AM EDT

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

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

Thu, Apr 4, 10:00 AM EDT

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Hauptbild für Medical Device Electrical Safety

Medical Device Electrical Safety

Mon, Mar 25, 10:00 AM EDT

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

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

Tue, Mar 5, 10:00 AM EST

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Hauptbild für BUNDLE: (EU) MDR 2017/745 and Technical Documentation per (EU) MDR 2017/745

BUNDLE: (EU) MDR 2017/745 and Technical Documentation per (EU) MDR 2017/745

Tue, Jan 30, 10:00 AM EST

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Hauptbild für European Medical Devices Regulation (EU) 2017/745

European Medical Devices Regulation (EU) 2017/745

Tue, Jan 30, 10:00 AM EST

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Hauptbild für Medical Device Single Audit Program (MDSAP) for Manufacturers

Medical Device Single Audit Program (MDSAP) for Manufacturers

Mon, Jan 22, 9:30 AM EST

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

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

Wed, Nov 1, 12:00 PM EDT

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

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

Mon, Oct 30, 10:00 AM EDT

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Hauptbild für European Medical Devices Regulation (EU) 2017/745

European Medical Devices Regulation (EU) 2017/745

Wed, Sep 27, 10:00 AM EDT

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

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

Wed, Aug 23, 10:00 AM EDT

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

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

Wed, Jul 26, 10:00 AM EDT

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Events

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

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

Tue, Sep 24, 10:00 AM EDT

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

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

Tue, Sep 24, 10:00 AM EDT

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

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

Tue, Apr 9, 9:00 AM EDT

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

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

Thu, Apr 4, 10:00 AM EDT

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Hauptbild für Medical Device Electrical Safety

Medical Device Electrical Safety

Mon, Mar 25, 10:00 AM EDT

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

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

Tue, Mar 5, 10:00 AM EST

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Hauptbild für BUNDLE: (EU) MDR 2017/745 and Technical Documentation per (EU) MDR 2017/745

BUNDLE: (EU) MDR 2017/745 and Technical Documentation per (EU) MDR 2017/745

Tue, Jan 30, 10:00 AM EST

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Hauptbild für European Medical Devices Regulation (EU) 2017/745

European Medical Devices Regulation (EU) 2017/745

Tue, Jan 30, 10:00 AM EST

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Hauptbild für Medical Device Single Audit Program (MDSAP) for Manufacturers

Medical Device Single Audit Program (MDSAP) for Manufacturers

Mon, Jan 22, 9:30 AM EST

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

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

Wed, Nov 1, 12:00 PM EDT

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

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

Mon, Oct 30, 10:00 AM EDT

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Hauptbild für European Medical Devices Regulation (EU) 2017/745

European Medical Devices Regulation (EU) 2017/745

Wed, Sep 27, 10:00 AM EDT

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

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

Wed, Aug 23, 10:00 AM EDT

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

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

Wed, Jul 26, 10:00 AM EDT

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

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

Tue, Apr 9, 9:00 AM EDT

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

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

Thu, Apr 4, 10:00 AM EDT

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Hauptbild für Medical Device Electrical Safety

Medical Device Electrical Safety

Mon, Mar 25, 10:00 AM EDT

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

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

Tue, Mar 5, 10:00 AM EST

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Hauptbild für BUNDLE: (EU) MDR 2017/745 and Technical Documentation per (EU) MDR 2017/745

BUNDLE: (EU) MDR 2017/745 and Technical Documentation per (EU) MDR 2017/745

Tue, Jan 30, 10:00 AM EST

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Hauptbild für European Medical Devices Regulation (EU) 2017/745

European Medical Devices Regulation (EU) 2017/745

Tue, Jan 30, 10:00 AM EST

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Hauptbild für Medical Device Single Audit Program (MDSAP) for Manufacturers

Medical Device Single Audit Program (MDSAP) for Manufacturers

Mon, Jan 22, 9:30 AM EST

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

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

Wed, Nov 1, 12:00 PM EDT

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

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

Mon, Oct 30, 10:00 AM EDT

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Hauptbild für European Medical Devices Regulation (EU) 2017/745

European Medical Devices Regulation (EU) 2017/745

Wed, Sep 27, 10:00 AM EDT

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

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

Wed, Aug 23, 10:00 AM EDT

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

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

Wed, Jul 26, 10:00 AM EDT

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