Care

FDA Authorizes ZYN as First Modified Risk Nicotine Pouch
Care FDA Authorizes ZYN as First Modified Risk Nicotine Pouch

The recent decision by the Food and Drug Administration to grant a modified risk tobacco product designation to ZYN marks a transformative moment in the landscape of nicotine regulation and harm reduction strategies. This move reflects a broader regulatory shift toward recognizing non-combustible

How Can Global Patient Support Programs Succeed Locally?
Care How Can Global Patient Support Programs Succeed Locally?

A patient residing in a remote area might find themselves struggling to navigate the complexities of a life-saving biologic therapy simply because the digital support platform was designed with a major metropolitan hub in mind, overlooking the specific connectivity and language nuances of their

How Is Telehealth Reshaping Veteran Mental Health Care?
Care How Is Telehealth Reshaping Veteran Mental Health Care?

For a generation of service members, the walk from the parking lot to a sterile VA clinic often felt longer and more daunting than the deployment that necessitated the visit in the first place. This physical and psychological distance has historically served as a silent gatekeeper, inadvertently

AI Drug Discovery Faces a $60 Billion Clinical Verdict
Care AI Drug Discovery Faces a $60 Billion Clinical Verdict

As a veteran of the life sciences industry with over two decades of experience navigating the complex corridors of the NIH and top-tier consultancies like Monitor Deloitte, I have witnessed firsthand the cyclical nature of biotech hype. The current fervor surrounding artificial intelligence in drug

America Needs a National Strategy for Headache Disorders
Care America Needs a National Strategy for Headache Disorders

The persistent and debilitating nature of headache disorders has influenced the trajectory of American history since the founding of the republic, yet these conditions remain largely sidelined by federal health policy. Thomas Jefferson, one of the nation’s most prominent architects, frequently d

FDA Backs UniQure Gene Therapy for Huntington’s Disease
Care FDA Backs UniQure Gene Therapy for Huntington’s Disease

The landscape of neurodegenerative medicine shifted dramatically in mid-June 2026 when the U.S. Food and Drug Administration signaled its readiness to accept an accelerated approval filing for UniQure’s experimental gene therapy. This specific development offers a critical lifeline to thousands of p

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