Past Events
Categories
Past event
VivaTech
Past event
Conferences
AMDM IVD Regulatory Submission Workshop
Past event
Conferences
OSMA 2026 Spring Meeting
Past event
Webinars
IVDR Proposed Revision: Practical Breakdown & Implications for IVD Manufacturers
Past event
Webinars
RWE-Driven MedTech: Cross-Sector Perspectives on Building Cost-Effective Clinical Evidence Strategies
Past event
Conferences
2026 US Medical Device & Diagnostic Post-Market Surveillance, Vigilance Conference
Past event
Fairs
The 34th China International Health Industry Expo 2026
Past event
Fairs
Hong Kong International Medical and Healthcare Fair
Past event
Fairs
Shanghai International Medical Devices Exhibition 2026
Past event
Fairs
Medical Fair China 2026
Past event
Fairs
RAPS Euro Convergence 2026
Past event
Conferences
2026 US Medical Device & Diagnostic Clinical Evidence Conference
GMED at the 2026 US Medical Device & Diagnostic Clinical Evidence Conference 24–26 March 2026 | Boston, MA GMED (...)
Past event
Fairs
The 23rd China International In Vitro Diagnostic Expo
Past event
Fairs
China International Medical Equipment Fair (CMEF)
Past event
Training
Biocompatibility of Medical Devices
Past event
Conferences
GMED at the Global Regulatory Strategy Conference in Baltimore
GMED is pleased to announce that Shahriar Sharifi and Florianne Torset-Bonfillou will be representing our organization at the forthcoming Global (...)
Past event
Webinars
2026 Regulatory Roadmap: Key MDR & IVDR Compliance Priorities
Past event
Training
Clinical investigation of medical devices
Past event
Training
Radiation sterilization of medical devices
Past event
Training
Medical Device Software Lifecycle per IEC 62304
Past event
Training
Systematic Literature Review for Medical Devices
Past event
Training
Technical Documentation per Medical Devices Regulation (EU) 2017/745
Past event
Training
Technical Documentation per In Vitro Diagnostic Devices Regulation (EU) 2017/746
Past event
Training
Technical Documentation per In Vitro Diagnostic Devices Regulation (EU) 2017/746
Past event
Training
Technical Documentation per In Vitro Diagnostic Devices Regulation (EU) 2017/746
Past event
Training
European in Vitro Diagnostic Devices Regulation (EU) 2017/746
Past event
Conferences
Veeva MedTech EU Summit 2025
Past event
Fairs
MedFIT
Past event
Conferences
9th Annual Medical Device Postmarket Surveillance Conference
Past event
Fairs
RAPS Convergence 2025
Past event
Conferences
MedTech Summit
Past event
Webinars
Practical Approach to Implementing LEAN Strategies for QMS Optimization
Past event
Conferences
2nd Annual US Medical Device & Diagnostic Post-Market Surveillance & Vigilance Conference
Past event
Webinars
Medtech market in Japan
Past event
Conferences
9th European Congress on implantable technologies
Past event
Training
Biocompatibility of Medical Devices Training
Past event
Conferences
OSMA Winter Meeting 2025
Past event
Fairs
TOPRA Symposium 2025
Past event
Fairs
The MedTech Forum 2025
Past event
Fairs
RAPS Euro Convergence 2025
Past event
Training
Post Market Surveillance and Vigilance
Past event
Training
The Clinical Evaluation Report (CER) requirements under the EU MDR 2017/745
Past event
Training
Bundle: European Medical Devices Regulation (EU) 2017/745 & Technical Documentation per Medical Devices (EU) 2017/745
Past event
Fairs
MedFIT 2024
Past event
Conferences
France Local Networking Group Virtual Event: Use of standards in the US and EU regulatory MD and IVDs framework
Past event
Conferences
Metrology for Health Regulation
Past event
Conferences
IVD Regulation and Software
Past event
Conferences
Regulation, Clinical and Software for Medical Devices
Past event
Conferences
15th Annual Medical Device & Diagnostic Labeling Conference
Past event
Conferences
Global Access 2024
Past event
Conferences
TEAM-PRRC THIRD ANNUAL SUMMIT
Past event
Conferences
26th Management Committee Meeting of the IMDRF
Past event
Training
Cleanliness of Newly Manufactured Medical Devices
Past event
Fairs
US RAPS Convergence 2024
Past event
Conferences
US Annual Medical Device Clinical Forum
Past event
Conferences
Q1 Productions: 14th Annual Medical Device & Diagnostic Labeling Conference
Past event
Conferences
Q1 Productions: 17th IVD Clinical & Regulatory Affairs Conference
Past event
Conferences
US Annual Medical Device and Diagnostic Post-Market Surveillance & Vigilance Conference
Past event
Training
Bundle: European IVDR (EU) 2017/746 & Technical Documentation per IVDR (EU) 2017/746
Past event
Training
Bundle: European Medical Devices Regulation (EU) 2017/745 & Technical Documentation per Medical Devices (EU) 2017/745
Past event
Conferences
16th IHPBA 2024 World Congress
Past event
Conferences
MedTech Summit 2024
Past event
Fairs
The MedTech Forum 2024
Past event
Fairs
MedtecLIVE 2024
Past event
Fairs
Euro RAPS Convergence 2024
Past event
Fairs
Médi’Nov Connection 2024
Past event
Fairs
MedTech Meetup 2024
Past event
Conferences
OSMA 2024 Winter Training
Past event
Conferences
US Annual Medical Device Human Factors and Usability Engineering Conference
Past event
Training
The Clinical Evaluation Report (CER) requirements under the EU MDR 2017/745
Past event
Training
Post Market Surveillance and Vigilance
Past event
Conferences
13th Annual Medical Device & Diagnostic Labeling Professional Education Course
Past event
Training
Medical Device Electrical Safety (a1/a2)
Past event
Conferences
5th Annual EU Medical Device Regulation Conference
Past event
Conferences
13th Annual Medical Device & Diagnostic Labeling Conference
Past event
Conferences
DeviceTalks Boston 2023
Past event
Conferences
5th Annual EU IVD Clinical & Regulatory Conference
Past event
Conferences
RAPS Convergence 2023
Past event
Training
European in Vitro Diagnostic Devices Regulation (EU) 2017/746
Past event
Training
European in Vitro Diagnostic Devices Regulation (EU) 2017/746
Past event
Training
Technical Documentation per Medical Devices Regulation (EU) 2017/745
Past event
Conferences
5th Annual Life Science Regulatory Intelligence & Strategy Conference
Past event
Conferences
RAPS Euro Convergence 2023
Past event
Conferences
16th annual IVD Clinical & Regulatory Affairs Conference
Past event
Conferences
BioHive Summit
Past event
Training
ISO 13485:2016 Requirements
Past event
Training
Medical Device Electrical Safety (A Review of IEC 60601-1/A2)
IEC 60601-1 3rd Edition represents the benchmark for medical electrical equipment and compliance to the standard is a requirement (...)
Past event
Conferences
MedTech Summit US
Past event
Training
Répondre aux exigences réglementaires en matière de surveillance après commercialisation et vigilance
Past event
Training
ISO 13485:2016 Requirements
Past event
Webinars
UKCA: Where we are and where we are going?
Past event
Conferences
The MedTech Forum
Past event
Training
Medical Device Electrical Safety (IEC 60601-1 3rd Edition)
IEC 60601-1 3rd Edition represents the benchmark for medical electrical equipment and compliance to the standard is a requirement (...)
Past event
Forum
IVDMD Forum
Implementation of Regulation (EU) 2017/746
Past event
Training
European Medical Device Regulation (EU) 2017/745
Past event
Training
Risk Management Applied to Medical Devices (ISO 14971:2019)
Past event
Training
European Medical Device Regulation (EU) 2017/745
Past event
Training
Medical Device Single Audit Program (MDSAP) for Manufacturers
Past event
Training
Risk Management Applied to Medical Devices (ISO 14971:2019)
Past event
Conferences
Medical Device Electrical Safety (IEC 60601-1 3rd Edition)
IEC 60601-1 3rd Edition represents the benchmark for medical electrical equipment and compliance to the standard is a requirement (...)
Past event
Forum
2019 GMED North America Forum
Past event
Transition to ISO 13485:2016, 1 Day Course.
Past event
Conferences
Convergence 2020 I RAPS
Save the date! GMED is coming into force at #RAPS2020.
Past event
Conferences
RAPS 2017
Past event
Key changes in MD & IVD regulations, transition and impacts for Medical Device manufacturers
Past event
FREE Webinar, Embedded Software in Medical Device: Common Regulatory and Quality pitfalls
Past event
CE Marking of Medical Devices: Elements to be provided during the Evaluation of the Technical Documentation
Past event
Conferences
RAPS Regulatory Convergence 2
The Regulatory Convergence Conference by RAPS is an annual multi-day gathering of the global regulatory community, the perfect opportunity (...)
Past event
RAPS Regulatory Convergence 3
The Regulatory Convergence Conference by RAPS is an annual multi-day gathering of the global regulatory community, the perfect opportunity (...)
Past event
Forum
RAPS Regulatory Convergence 4
The Regulatory Convergence Conference by RAPS is an annual multi-day gathering of the global regulatory community, the perfect opportunity (...)
Past event
Conferences
RAPS Regulatory Convergence 5
The Regulatory Convergence Conference by RAPS is an annual multi-day gathering of the global regulatory community, the perfect opportunity (...)
Past event
Conferences
RAPS Regulatory Convergence 6
The Regulatory Convergence Conference by RAPS is an annual multi-day gathering of the global regulatory community, the perfect opportunity (...)
Past event
RAPS Regulatory Convergence 7
The Regulatory Convergence Conference by RAPS is an annual multi-day gathering of the global regulatory community, the perfect opportunity (...)
Past event
Forum
Medical Device Electrical Safety (IEC 60601-1 3rd Edition)
IEC 60601-1 3rd Edition represents the benchmark for medical electrical equipment and compliance to the standard is a requirement (...)
Past event
Webinars
RAPS Regulatory Convergence 1
The Regulatory Convergence Conference by RAPS is an annual multi-day gathering of the global regulatory community, the perfect opportunity (...)