MDR Certification Strengthens Resyca’s Leadership in Soft Mist Drug-Device Combination Products ENSCHEDE, NL / ACCESS ...

The U.S. Food and Drug Administration (FDA) said on Thursday it had identified three cybersecurity risks associated with ...

MDR Certification Strengthens Resyca's Leadership in Soft Mist Drug-Device Combination Products ENSCHEDE, NL / ACCESS Newswire / January 28, 2025 / Resyca BV, a pioneering leader in the development an ...

What will the industry face or achieve in 2025? These trends will be critical in medical device cybersecurity.

In the United States, the biomedical industry encounters numerous regulatory challenges in conducting nonclinical and ...

The website changes raise concerns about “the interference of politics with the study and the practice” of science and ...

Beta CEO Marcel Botha talks about the FDA’s plans for medical shortage notifications and how Trump’s policies may impact US ...

In the EU, the AI Act has been approved, carrying significant implications for medical device, technology, and pharmaceutical firms. In the US, ...

While experts across the political spectrum are generally in favor of stricter regulations ... FDA classifies most beauty products as low risk to health as compared to drugs and medical devices.

Dr. Sara Brenner, who has been FDA CDRH's in vitro diagnostics chief medical officer, is serving as acting commissioner of the agency.

Medical Device Market Size was estimated at USD 335428.32 million in 2024 and it is expected to grow from USD 354883.17 million in 2025 to USD 397243.44 million by 2033. The Market CAGR (growth rate) ...

The US Food and Drug Administration (FDA) has named Sara Brenner, a physician and senior official in its medical device ...