Traditionally, contract negotiation has been viewed as a financial or legal responsibility, typically led by finance teams, ...

The FDA has approved the NEXUS Aortic Arch Stent Graft enabling commercial launch of the NEXUS System in the US.

InVera Medical has received FDA 510 (k) clearance for the InVera Infusion Device, a new minimally invasive device designed to ...

E. Almeida as Chief Executive Officer, effective immediately upon closing of the previously announced company acquisition.

Designed to expand treatment options for patients with cirrhosis and complications of portal hypertension, this ...

Companies and researchers often fail to disclose negative trial results, resulting in significant gaps in the public record ...

Allevion Medical Receives FDA Clearance for Vantage™, Introducing a Fully Disposable Approach to Minimally Invasive Spinal ...

As organizations introduce additional technologies, including AI-enabled tools and CRM platforms, these gaps become more ...

Serenity Medical announced FDA Humanitarian Device Exemption (HDE) approval for its novel River stent. The River stent is for the treatment of severe idiopathic intracranial hypertension (IIH) in ...

New set of 73 Real World Evidence examples illustrate how RWD can support rigorous validation of novel device software functions across multiple disease areas. By: Daniel Caños, Ph.D., MPH, Director, ...