Upcoming Events
Events
Find an answer to the challenges you are facing in one of our upcoming events: trainings, webinars, forums…
Categories
Mar 27, 2025 AKRA TEAM & MedTech Leading Voice
Webinars
Practical Approach to Implementing LEAN Strategies for QMS Optimization
Apr 01 - 02, 2025 Training | Virtual Classroom
Trainings
The Clinical Evaluation Report (CER) requirements under the EU MDR 2017/745
Apr 15 - 16, 2025 Orthomanufacture | Basel, Switzerland
Conferences
9th European Congress on implantable technologies
Apr 22 - 24, 2025 Training | Virtual Classroom
Trainings
Medical Device Software Lifecycle per IEC 62304
May 13 - 15, 2025 MedTech Europe | Lisbon, Portugal
Fairs
The MedTech Forum
May 13 - 16, 2025 Regulatory Affairs Professionals Society | Brussels, Belgium
Fairs
RAPS Euro Convergence 2025
Jun 17 - 18, 2025 Training | Virtual Classroom
Trainings
Risk Management Applied to Medical Devices (ISO 14971:2019)
Jun 24 - Jul 17, 2025 Training | Virtual Classroom
Trainings
Bundle: European Medical Devices Regulation (EU) 2017/745 & Technical Documentation per Medical Devices (EU) 2017/745
Jul 15 - 17, 2025 Training | Virtual Classroom
Trainings
Technical Documentation per Medical Devices Regulation (EU) 2017/745
Jul 22 - 24, 2025 Training | Virtual
Trainings
Medical Device Electrical Safety
Jul 29 - 30, 2025 Training | Virtual Classroom
Trainings
Post Market Surveillance and Vigilance
Aug 05, 2025 Training | Virtual Classroom
Trainings
The Clinical Evaluation Report (CER) requirements under the EU MDR 2017/745
Aug 26 - 27, 2025 Training | Virtual Classroom
Trainings
Radiation Sterilization of Medical Devices
Sep 16 - 17, 2025 Training | Virtual Classroom
Trainings
European Medical Device Regulation (EU) 2017/745
Sep 16 - Oct 16, 2025 Training | Virtual Classroom
Trainings
Bundle: European Medical Devices Regulation (EU) 2017/745 & Technical Documentation per Medical Devices (EU) 2017/745
Sep 29 - Oct 01, 2025 TOPRA | Berlin, Germany
Fairs
TOPRA Symposium 2025
Sep 29 - Oct 03, 2025 Training | Virtual Classroom
Trainings
Medical Device Single Audit Program (MDSAP) for Manufacturers
Oct 14 - 16, 2025 Training | Virtual Classroom
Trainings
Technical Documentation per Medical Devices Regulation (EU) 2017/745
Oct 21, 2025 Training | Virtual Classroom
Trainings
The Clinical Evaluation Report (CER) requirements under the EU MDR 2017/745
Oct 28 - Nov 20, 2025 Training | Virtual Classroom
Trainings
Bundle: European IVDR (EU) 2017/746 & Technical Documentation per IVDR (EU) 2017/746
Oct 28 - 29, 2025 Training | Virtual Classroom
Trainings
European in Vitro Diagnostic Devices Regulation (EU) 2017/746
Nov 04, 2025 Training | Virtual Classroom
Trainings
Post Market Surveillance and Vigilance
Nov 18 - 20, 2025 Training | Virtual Classroom
Trainings
Technical Documentation per In Vitro Diagnostic Devices Regulation (EU) 2017/746
Dec 02 - 03, 2025 Training | Virtual Classroom
Trainings
Risk Management Applied to Medical Devices (ISO 14971:2019)
May 06 - 07, 2025 Training | Virtual Classroom
Trainings
Cleanliness of newly manufactured medical devices
Jun 05, 2025 The Juniper Room | GMED North America
Conferences
Unlocking the Potential of MDSAP – Quality, Regulatory, and Commercial Advantages
Jun 10 - 12, 2025 TT LifeSciences | Boston, Massachusetts
Conferences
2nd Annual US Medical Device & Diagnostic Post-Market Surveillance & Vigilance Conference
Jun 24 - 25, 2025 Training | Virtual Classroom
Trainings
European Medical Device Regulation (EU) 2017/745
Aug 12 - 14, 2025 Training | Virtual
Trainings