The Limestone County Emergency Management Agency said early Saturday morning that it has one outdoor warning siren still out of service and awaiting parts for repairs.

The EMA warns of products being sold as dendritic cell therapies with little evidence, but high health risks, in the European ...

The US Food and Drug Administration (FDA) has granted approval for Valcare Medical’s investigational device exemption application, allowing it to begin an early feasibility study of its transcatheter ...

The Goodsprings and Witty Mill outdoor warning sirens in Limestone County remain out of service, according to the Limestone County Emergency Management Agency.

Using Nvidia and GE Healthcare technology, the robotic surgery system is intended to help doctors detect lung cancer earlier.

Paragonix Technologies, a pioneer in organ transplant technologies and organ procurement services, announced today that five of its devices have now received approval under the European Union (EU) ...

The study found that just 20% of trials submitted to both the FDA and European Medicines Agency had matching evidence.

Femasys (FEMY) announces Conformite Europeene mark certification under European Union Medical Device Regulation as the first regulatory ...

Obtaining the Marketing Authorisation Application (MAA) is a key step in the commercialization of drugs in the EU, and also an important help to promote the global market expansion of pharmaceutical ...

Discover how outsourcing regulatory submission content development improves efficiency and ensures compliance.

Pfizer's Covid-19 vaccine is considered by healthcare authorities to be safe and effective, with data gathered from billions ...

The global preclinical medical device testing services market is poised for steady expansion, with revenue expected to grow from USD 1,696.0 million in 2025 to USD 2,842.1 million by 2035, at a CAGR ...