IMDRF Trainings
In accordance with the IMDRF 2021-2025 Strategic Plan, IMDRF is taking additional steps to further promote regulatory convergence. One of the identified pathways to achieving this goal is the development of training programs which aim to facilitate a consistent understanding and implementation of IMDRF technical documents.
As a first step, the 'Adverse Event Terminology Training Pilot' aims to deliver on a web-based publicly accessible training on the IMDRF N43 Technical Document titled 'IMDRF terminologies for categorised Adverse Event Reporting (AER) - Terms, terminology structure and codes'. Understanding Adverse Event Reporting is an essential part of ensuring that medical devices on the market are appropriately reported upon should post-market issues and incidents arise. This training may be considered of use to regulatory authorities, manufacturers as well as healthcare institutions.
For any further details on IMDRF Trainings, please email the IMDRF Secretariat.
