When conducting a clinical investigation, meeting regulatory requirements is predicated on factors such as the quality of data input.

Nasal vaccine devices have the potential to offer more convenient and more effective protection against a variety of viruses.

The 2024 study, of 202 regulatory professionals at Class 2 and 3 medical device companies in the EU (Germany) and North America (the US), started by reviewing medical device suppliers ...

Its expansion is attributed to increasing regulatory requirements. The global preclinical medical device testing services ...

Several executive orders recently signed by US President Donald Trump may have significant implications for the US Food and Drug Administration ...

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

The "Medical Device Regulatory Affairs Market Size, Share & Trends Analysis Report By Type, By Service Provider, By Service, By Region, And Segment Forecasts, 2025 - 2030" report has been added to ...

The Brazilian Health Regulatory Agency (ANVISA) granted approval for the FlareHawk7 and FlareHawk9 spine implant devices.

Trace - True Ray Tracing Aberrometer and Topographer Tracey Technologies announced that the company has successfully achieved certificatio ...

The "Market Authorisation of Software as a Medical Device (SaMD) and Medical Device Software (MDSW) Training Course (ONLINE EVENT: March 26-27, 2025)" has been added to ResearchAndMarkets.com's ...