Jan 12, 2024
Understanding IEC/ISO 62304 and FDA Requirements for Medical Device Software Development Life Cycle (SDLC) Management
Jan 12, 2024
Which EU Notified Bodies Have Been “Designated” Under the MDR 2017/745 and IVDR 2017/746?
Jan 12, 2024
MDCG 2022-6: Making Changes to Legacy Devices Without Triggering EU IVDR Compliance
Jan 12, 2024
Supplementing Your Medical Device PMS Efforts with Online Data
Jan 12, 2024
Preparing for a Notified Body Medical Device Clinical Audit
Jan 12, 2024
The New IVDR Compliance Deadline Extension Explained
