Preconference Workshops registration will close
Wednesday, 5 May at 5:00 pm EDT (23:00 CET).
Register now to gain exclusive content provided by EU regulatory experts.
Preconference workshops are a great way to enhance your Euro Convergence experience. These workshops focus on a singular area that provides an extensive, in-depth look into specific regulatory topics.
For 2021, there will be four optional preconference workshops that will occur on 7 May 2021. Please note that a separate fee is required to attend each preconference and is not included in the main registration for RAPS Euro Convergence 2021. There are 40 seats for each workshop, so seats are limited.
Post Market Reporting
Learn how to meet the MDR Post-Market Reporting requirements, specifically the new requirements under Article 88/Trending and Periodic Safety Update Reporting (PSUR).
Risk Management Under the EU Regulations for Medical Devices & In Vitro Diagnostics
Hear how to apply the risk management requirements from MDR and IVDR using ISO 14971:2019, including planning for and processing of postmarket surveillance data.
Software as a Medical Device
Review current and evolving regulatory requirements for Software as a Medical Device (SaMD), Software in a Medical Device (SiMD), and Medical Device Software (MDSW) with a focus on artificial intelligence-based medical devices.
Clinical Studies in PMCF
Gain insight into when a Post Market Clinical Investigation will be a suitable source of clinical data.