MTI Regulatory Report 2024 data overwhelmingly suggests regulatory resources throughout the industry are being stretched.

What are the essentials for compliant claims? How do you support and monitor claims in packaging and promotional content?

Fraudulent data is becoming more common by the submission. So much so that the FDA recently published a press release reminding medical device manufacturers to scrutinize Third-Party Generated Data.” ...

Modern interoperable systems, data centralization, and a wide-angle view of inventory and usage trends are providing ...

Five startups selected to participate in Memphis area Accelerator following The comprehensive 13-week go-to-market program is ...

Largest U.S. Prospective Clinical Trial Ever Conducted Demonstrated High Compliance with the Flexitouch® System and ...

MedTech organizations need to focus on the human factor of change and achieve top-down alignment, buy-in, accountability, and clear communication along the way. MEDICA 2024 and COMPAMED 2024 trade ...