Sign up for the QMED & MD+DI Daily newsletter.
Using Standards to Demonstrate Conformity
Using US, UK, and European MedTech standards to influence regulatory compliance
December 22, 2023
1 Min Read
Organizations that need to address “state of the art” regulatory requirements should monitor and understand the development of new or revised standards that affect their activities. How much effort, weight and resources allocated to standards implementation may vary by individual situations. This paper helps define the boundaries of those efforts and describes the process of standards development activities and their value and application.
You May Also Like
Pedersen's POV graphic featuring the headshot of MD+DI Senior Editor Amanda Pedersen and a pull quote from the latest edition of her opinion column.
The EU AI Act: How Will It Impact Medical Device Manufacturers?Feb 27, 2024|8 Min Read
BioSig's Ridiculously Sparse Layoff Announcement Reeks of CallousnessFeb 26, 2024|3 Min Read
Sourcing Electrical Components: Are We Back to Normal?Feb 26, 2024|6 Min Read
Your Smartwatch Can’t Measure Blood Glucose Levels… YetFeb 26, 2024|3 Min Read