Airborne ultrasound enables non-destructive seal monitoring, detecting subtle material variations. See how this proactive ...

Deterministic, non-destructive seal integrity testing delivers validated, quantitative results. Learn why this method ...

Advanced inspection technologies are redefining implant packaging integrity, reducing risks and improving efficiency. Learn ...

Preventing leaks and seal failures in sterile packaging is vital for patient safety. Learn how vacuum decay and airborne ...

Maintaining sterile packaging for CGMs is critical to patient safety. Explore advanced methods like vacuum decay and airborne ...

Defects in porous lidded trays can compromise sterility and patient safety. Discover how vacuum decay technology delivers non ...

Implantable systems offer precise, localized therapy, improving adherence. Overcoming biological barriers and surgical ...

Blurred lines between medical devices and wellness apps create risks. Developers must adopt robust privacy and security for ...

The wearable medical device industry sits at the intersection of life sciences regulation and rapidly-evolving technology law. Companies in this space face overlapping legal frameworks that can ...

Navigating the evolving landscape of global regulations concerning Per- and Polyfluoroalkyl Substances (PFAS) in medical devices requires a proactive, comprehensive strategy. Manufacturers must ...

An FDA warning letter is more than a formal notice; it’s a visible sign that a company’s quality system has failed to meet critical expectations. Yet behind every warning letter lies a wealth of ...

The global medical device market is estimated to be currently about $680 billion and is projected to grow to over a trillion dollars within 10 years at a compound annual growth rate of 6%. 1 As the ...