Jan 02, 2023
EU MDR Vigilance Reporting Requirements and MEDDEV 2.12-1 Rev 8
Oct 03, 2022
Medical Device Equivalence: How Close Does It Need to Be Under the EU MDR and MEDDEV 2.7/1 rev 4?
Aug 08, 2022
All Class 1 Medical Device Manufacturers Must Meet These Specific EU MDR Requirements
Mar 22, 2022
State of the Art in the EU MDR: What Does That Actually Mean?
Oct 12, 2021
eLabeling and eIFU Requirements Under the EU MDR and Regulation 2021/2226
Jun 02, 2021
You’ve Evaluated Every Risk But Are You Properly Documenting Medical Device Benefits?
