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On May 16, 2025, Grace Graham, deputy commissioner for policy, legislation and international affairs at the Food and Drug Administration (FDA), delivered a keynote address at the Food and Drug Law ...
The ultrasound catheter is being tested in the PreVail-PH2 study, an early feasibility trial enrolling PH patients with left ...
E-commerce and healthcare growth in the USA boosts demand for durable, eco-friendly moulded pulp packaging to protect ...
Key Takeaways - The Federal Trade Commission (FTC), now under Republican leadership, has continued its scrutiny of Orange Book ...
A new treatment option has emerged for patients battling advanced squamous cell carcinoma of the anal canal (SCAC). The U.S.
FDA chief pushes back on senators’ criticism, says Covid booster trials should take ‘roughly a year’
The hearing was supposed to focus on the Trump administration’s 2026 budget request, but instead covered a wide range of ...
The FDA plans to limit access to certain high-risk groups and also told Pfizer and Moderna to update their warning labels ...
1d
Medical Device Network on MSNReGelTec’s system for disc augmentation gains CE Mark approvalThe approval is based on a trial that revealed that the system’s treatment led to improvements in disability and pain.
A band of clinicians and chronic pain advocates are pushing regulators to scrutinize a controversial risk rating tool.
In this week’s edition of InnovationRx, we look at the FDA's new rules on Covid-19 vaccines, Novartis’s acquisition strategy, ...
Recent FDA updates in the areas of cardiac intervention, hypertension and arrhythmia disorders expand the pool of available ...
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