US tariffs on medical devices: What manufacturers need to consider now On April 9, 2025, the US government surprisingly announced a 90-day pause in tariffs. [...]
US tariffs on medical devices: What manufacturers need to consider now Read More "
Regulatory overlaps in medical technology: MDR/IVDR, AI Act and data protection in focus The integration of artificial intelligence (AI) in medical devices
MDR/IVDR, AI Act & data protection - the magic triangle Read More "
Regulatory resilience as a success factor for the global market access of medical devices In an increasingly complex regulatory landscape, manufacturers of medical devices are faced with a number of challenges.
Regulatory resilience as a success factor Read More "
QMSR replaces QSR: What medical device manufacturers need to know now From February 2, 2026, a new regulatory framework will apply in the USA.
QMSR replaces QSR: What medical device manufacturers need to know now Read More "
Medtech market 2025: trends, challenges and how manufacturers can remain successful The medical technology industry in Germany is facing a challenging year in 2025.
Medtech market 2025: How manufacturers remain successful Read More "
MDR Ready - What importers and distributors need to consider now Regulation (EU) 2017/745 (Medical Device Regulation, MDR) has been in force since
MDR Ready - What importers and retailers need to consider Read More "
