In the latest MDR Chats episode, we dive into the new guidance on Article 10a covering manufacturers' obligations for supply interruptions and discontinuations.
Highlights:
Essential timelines and reporting duties
Risk factors impacting patient safety
What qualifies as “exceptional circumstances”
Join Dr. Emily Bennett and host Oliver Harris to understand what these changes mean for medical device compliance in the EU.
Podden och tillhörande omslagsbild på den här sidan tillhör
ChatMDR. Innehållet i podden är skapat av ChatMDR och inte av,
eller tillsammans med, Poddtoppen.