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Sep 29 - 30, 2026 Training | Virtual Classroom
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Medical Device Single Audit Program (MDSAP) for Manufacturers
Oct 06 - 07, 2026 Training | Virtual Classroom
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ISO 13485:2016 Requirements
Oct 13 - 14, 2026 Training | Virtual Classroom
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Technical Documentation per Medical Devices Regulation (EU) 2017/745
Oct 21, 2026 Training | Virtual Classroom
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The Clinical Evaluation Requirements (CER) under the EU MDR 2017/745
Nov 10, 2026 Training | Virtual Classroom
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Post Market Surveillance and Vigilance
Nov 18, 2026 Training | Virtual Classroom
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Clinical investigation of medical devices
Nov 18 - 19, 2026 Training | Virtual Classroom
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European in Vitro Diagnostic Devices Regulation (EU) 2017/746
Dec 01 - 02, 2026 Training | Virtual Classroom
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Risk Management Applied to Medical Devices (ISO 14971:2019)
Dec 09 - 10, 2026 Training | Virtual Classroom
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Technical Documentation per In Vitro Diagnostic Devices Regulation (EU) 2017/746
Dec 10 - 11, 2026 Training | Virtual
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Biocompatibility of Medical Devices
Feb 02 - 03, 2027 Training | Virtual Classroom
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European Medical Device Regulation (EU) 2017/745
Feb 09 - 10, 2027 Training | Virtual Classroom
Training
European in Vitro Diagnostic Devices Regulation (EU) 2017/746
Feb 23 - 24, 2027 Training | Virtual Classroom
Training
Risk Management Applied to Medical Devices (ISO 14971:2019)
Mar 02, 2027 Training | Virtual
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Systematic Literature Review for Medical Devices
Mar 09, 2027 Training | Virtual Classroom
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Post Market Surveillance and Vigilance
Mar 16 - 17, 2027 Training | Virtual Classroom
Training
Technical Documentation per Medical Devices Regulation (EU) 2017/745
Mar 30 - 31, 2027 Training | Virtual Classroom
Training
Technical Documentation per European In Vitro Diagnostic Device Regulation (EU) 2017/746
Apr 06 - 07, 2027 Training | Virtual Classroom
Training
Medical Device Single Audit Program (MDSAP) for Manufacturers
Apr 13 - 14, 2027 Training | Virtual Classroom
Training
ISO 13485:2016 Requirements
Apr 20, 2027 Training | Virtual Classroom
Training
The Clinical Evaluation Report (CER) requirements under the EU MDR 2017/745
Apr 27 - 28, 2027 Training | Virtual Classroom
Training
European in Vitro Diagnostic Devices Regulation (EU) 2017/746
May 04 - 05, 2027 Training | Virtual
Training
Medical Device Software Lifecycle per IEC 62304
May 11 - 12, 2027 Training | Virtual
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Biocompatibility of Medical Devices
May 18 - 19, 2027 Training | Virtual Classroom
Training
Technical Documentation per European In Vitro Diagnostic Device Regulation (EU) 2017/746
May 25 - 26, 2027 Training | Virtual Classroom
Training
Cleanliness of Newly Manufactured Medical Devices
Jun 08 - 09, 2027 Training | Virtual Classroom
Training
ISO 13485:2016 Requirements
Jun 15 - 16, 2027 Training | Virtual Classroom
Training
European Medical Device Regulation (EU) 2017/745
Jun 22 - 23, 2027 Training | Virtual Classroom
Training
European in Vitro Diagnostic Devices Regulation (EU) 2017/746
Jun 29 - 30, 2027 Training | Virtual Classroom
Training
Risk Management Applied to Medical Devices (ISO 14971:2019)
Jul 13, 2027 Training | Virtual Classroom
Training
Post Market Surveillance and Vigilance
Jul 20 - 21, 2027 Training | Virtual Classroom
Training
Technical Documentation per Medical Devices Regulation (EU) 2017/745
Jul 27 - 28, 2027 Training | Virtual Classroom
Training
Technical Documentation per European In Vitro Diagnostic Device Regulation (EU) 2017/746
Aug 03 - 04, 2027 Training | Virtual
Training
Medical Device Electrical Safety
Aug 10, 2027 Training | Virtual Classroom
Training
The Clinical Evaluation Report (CER) requirements under the EU MDR 2017/745
Aug 17 - 18, 2027 Training | Virtual
Training
Biocompatibility of Medical Devices
Aug 24 - 25, 2027 Training | Virtual
Training
Radiation sterilization of medical devices
Aug 31 - Sep 01, 2027 Training | Virtual Classroom
Training
European Medical Device Regulation (EU) 2017/745
Sep 14, 2027 Training | Virtual
Training
Systematic Literature Review for Medical Devices
Sep 21 - 22, 2027 Training | Virtual Classroom
Training
Medical Device Single Audit Program (MDSAP) for Manufacturers
Sep 28 - 29, 2027 Training | Virtual Classroom
Training
Technical Documentation per Medical Devices Regulation (EU) 2017/745
Oct 12 - 13, 2027 Training | Virtual
Training
Medical Device Software Lifecycle per IEC 62304
Oct 19 - 20, 2027 Training | Virtual Classroom
Training
European in Vitro Diagnostic Devices Regulation (EU) 2017/746
Oct 26, 2027 Training | Virtual Classroom
Training
Post Market Surveillance and Vigilance
Nov 02 - 03, 2027 Training | Virtual Classroom
Training
ISO 13485:2016 Requirements
Nov 09 - 10, 2027 Training | Virtual Classroom
Training
Risk Management Applied to Medical Devices (ISO 14971:2019)
Nov 16 - 17, 2027 Training | Virtual Classroom
Training
Technical Documentation per European In Vitro Diagnostic Device Regulation (EU) 2017/746
Nov 30 - Dec 01, 2027 Training | Virtual
Training
Biocompatibility of Medical Devices
Dec 07, 2027 Training | Virtual Classroom
Training