There’s been a lot of buzz surrounding the cardiovascular market, lately. From deals reaching into the billions to breakout data there’s no denying all eyes are on the cardiovascular space. MD+DI has ...

This week marks an important anniversary in medtech: The 11th anniversary of transcatheter aortic valve replacement (TAVR) being approved by FDA. The agency announced on November 2, 2011 that it had ...

Medtronic announced not one, not two, but three significant regulatory approvals for its Hugo robotic-assisted surgery (RAS) system this week. The Dublin, Ireland-based company has received CE mark ...

On the heels of launching Omnipod 5 in the United States, Insulet has received CE marking to sell the device in Europe. The Omnipod 5 is the first CE marked tubeless hybrid closed loop system (also ...

The COVID-19 outbreak has forced rapid adaptation across the entire healthcare industry. With a dire need for medical devices and personal protective equipment (PPE), manufacturers have quickly sought ...

After evaluating more than 100 products submitted to the 2000 Medical Design Excellence Awards (MDEA) competition, a jury of medical device industry experts has selected 29 finalists representing the ...

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Duane Morris Silicon Valley office partner Agatha H. Liu, PhD, practices intellectual property law, focusing on IP analysis, portfolio management, and strategic counseling. Drawing on more than 20 ...

A camera-carrying pill may soon be available as a painless alternative to invasive gastrointestinal endoscopy. The disposable capsule, which will be marketed by Given Imaging Ltd. (Yokneam, Israel), ...

In December 2014, OtisMed Corporation agreed to pay more than $80 million after acknowledging that the company and its ex-CEO knowingly sold surgical cutting guides for knee replacements even though ...

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To put it simply, the purpose of validating any software or computerized system is to establish trust in the data or electronic record. Spreadsheets and databases are automated data processing systems ...