Acquisition to expand cardiovascular portfolio with complementary and differentiated calcium modification platform, ...

According to CDER Director Patrizia Cavazzoni, CDER’s new Center for Real-World Evidence Innovation represents a major step ...

Acquisition expected to strengthen Stryker's neurovascular business with Inari VTE product portfolio including mechanical ...

The European Commission’s Green Deal sets specific sustainability targets across the EU, while policies like the German ...

In a document updated for the first time since 2017, AAMI released new guidance for EO material compatibility and including ...

Harmony™ Transcatheter Pulmonary Valve system received approval for minimally invasive treatment option for patients with ...

Advancements in cardiac care and novel therapies are transforming cardiac medical devices, providing new solutions for ...

Computerized Maintenance Management System (CMMS) software can be a vital tool for life sciences manufacturers in maintaining ...

The United States is currently under the spotlight as Donald Trump’s recent appointment and consequent nomination of Robert F ...

Fraudulent data is becoming more common by the submission. So much so that the FDA recently published a press release reminding medical device manufacturers to scrutinize Third-Party Generated Data.” ...

Law firm, Hogan Lovells, analyzes the changes to the updated enforcement policy and provide key takeaways for entities responsible for communication regarding approved/cleared medical products.