FDA
The Focalist system aims to combine handheld robotics with real-time imaging to enable clinicians to place needles more precisely.
The company will use the funds for a European feasibility study for its transcatheter device and for the launch of a U.S.-based clinical study.
Cirrus uses fMRI imaging to acquire and generate maps of critical brain networks to assist with brain surgery planning.
Elsa provides a secure platform for scientific reviewers and investigators to access internal documents.
The next-generation Swoop system software enhances image quality for ultra-low-field magnetic resonance imaging.
New NIH office will promote human-based research and scale the use of non-animal approaches to biomedical research.
Lilly accuses four compounders of selling unauthorized versions of the pharma giant's diabetes and weight-loss drugs.
Data from the clinical trial might give patients a new option for treating migraines.
Ben Wolf, partner in Alston & Bird's Health Care Group, told MobiHealthNews how FDA staffing cuts could slow device approvals and what companies can do to stay ahead.
The judge ruled that the FDA overstepped its authority by regulating LDTs as medical devices, overturning the rule and remanding it to the HHS Secretary for review.