Consumer
It confidently relies on expert knowledge based on two decades of research with young people.
The quarter marks the first time the company reported profitability on an adjusted EBITDA basis.
The company's Dream Sock, which received FDA 510(k) clearance in November, gathers real-time health readings, including a baby's sleep trends and pulse rate.
The announcement comes less than a year after Virgin Pulse and HealthComp announced their $3 billion merger and their rebranding as Personify Health.
The Agency has qualified Apple's atrial fibrillation history feature as a medical device development tool, allowing it to be used in clinical trials.
The open-source gene editor is freely available to license for commercial use and ethical research.
The Agency alleges the company's CT and ultrasonography systems are noncompliant with good manufacturing requirements.
Dr. Julia Frydman will be the oncology-focused company's first medical director for palliative care. She will oversee its new Enhanced Supportive Care program.
The new platform for will offer video visits for rare disease diagnosis and longitudinal care.
Business model is unsustainable due to a challenging reimbursement environment and escalating operating costs, company says.