What Notified Bodies Look for in EU MDR Technical Documentation What Notified Bodies Look for in EU MDR Technical Documentation Read More »
Navigating the Medical Device Market Entry Gameplan: The EU and The US Analysis Navigating the Medical Device Market Entry Gameplan: The EU and The US Analysis Read More »
EU MDR Cybersecurity Requirements for Medical Devices EU MDR Cybersecurity Requirements for Medical Devices Read More »
CE Marking for Software as Medical Device (SaMD) CE Marking for Software as Medical Device (SaMD) Read More »
EU Declaration of Conformity for Medical Devices: All You Need to Know EU Declaration of Conformity for Medical Devices: All You Need to Know Read More »
The Importance of CE Marking for Ophthalmic Medical Devices The Importance of CE Marking for Ophthalmic Medical Devices Read More »
‘Sell-Off Dates’ Removal Finalised: Extension to EU MDR Transition Periods ‘Sell-Off Dates’ Removal Finalised: Extension to EU MDR Transition Periods Read More »
Don’t procrastinate due to the EU MDR Transition extension : Results may be Costlier Don’t procrastinate due to the EU MDR Transition extension : Results may be Costlier Read More »