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| Episode | Date |
|---|---|
|
MDCG2025-6-Interplay Between MDR, IVDR, and the AI Act
|
Jul 03, 2025 |
|
MDCG 2025-4 -making available of MDSW apps on online platforms
|
Jun 25, 2025 |
|
Team-NB MDR Certification Consensus
|
Dec 19, 2024 |
|
MDCG 2019-13 Rev. 1: Understanding the Temporary Sampling Update
|
Dec 17, 2024 |
|
MDCG 2024-14-Master UDI-DI for Contact Lenses
|
Dec 05, 2024 |
|
MDCG 2024-15- clinical investigation in the absence of EUDAMED
|
Dec 05, 2024 |
|
AI in Medical Devices Questionnaire by the German NBs Alliance and Team NB
|
Nov 25, 2024 |
|
Gradual Roll-Out of EUDAMED
|
Nov 23, 2024 |
|
Supply Interruptions & Discontinuations: The New Information Obligation for Medical Devices and IVDs
|
Oct 30, 2024 |
|
MDR Requirements for Legacy Devices: Insights from the Latest MDCG Revision (MDCG 2021-25 Rev. 1)
|
Oct 29, 2024 |
|
MDCG 2024-13 - Regulatory status of ethylene oxide
|
Oct 29, 2024 |
|
MDR Conformity Assessment Routes:
|
Oct 27, 2024 |
|
Sufficient levels of access to data needed to justify claims of equivalence
|
Jul 05, 2024 |
|
Guidance on Standardisation for Medical Devices - Rev 1, Published July 2024
|
Jul 02, 2024 |
|
Clinical evaluation of orphan medical devices
|
Jun 30, 2024 |
|
Risk-Based Statistical Sampling Plan
|
May 04, 2024 |
|
A Deep Dive into Medical Device Deadlines
|
Apr 22, 2024 |
|
The Significance of the EU AI Act for Medical Devices
|
Mar 24, 2024 |
|
Person Responsible for Regulatory Compliance, PRRC
|
Mar 17, 2024 |
|
MDRChats | Official Trailer
|
Mar 17, 2024 |