MD+DI Senior Editor Amanda Pedersen explores the urgent need for transparency in medical device reporting, highlighting ...
On October 1, 2024, the Food and Drug Administration (FDA) marked a major milestone in medical device cybersecurity enforcement. This marks one year since the retracted Refuse to Accept (RTA) policy ...
Following is a synopsis of MD+DI’s conversation with Snell, in which he shared his thoughts on the MIPI A-PHY standard for ...
ZHUHAI CITY, GUANGDONG PROVINCE, CHINA, March 25, 2026 /EINPresswire.com/ -- The global endoscopy market continues to ...
Despite intensive medtech industry lobbying to secure a carve-out from the Trump administration’s expansive tariffs on all countries, medical devices have been swept up in the tariff net. Why it ...
Medical device makers are seeking an exemption from Donald Trump's tariffs they say will raise the price of their products and devastate the medical device and medical technology industry. In this ...
Medical device manufacturers urge the Indian government to expedite GST refunds and offer customs duty rebates amid rising ...
Opinion: Medical device companies can create a competitive advantage by leveraging data to strengthen compliance programs and ...
Americans cannot rely on the Food & Drug Administration (FDA) to guarantee that medical devices are safe, and a recent Government Accountability Office (GAO) report only strengthens that conclusion.
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