Hospital merger and acquisition activity ended 2025 with momentum expected to continue as drastic cuts to Medicaid spending under Trump’s One Big Beautiful Bill Act loom.
Blog
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FDA ImportShield Program Delivers Impressive Results in Strengthening FDA Oversight at U.S. Ports of Entry

The U.S. Food and Drug Administration today announced its initial review of the effectiveness of the FDA ImportShield Program (FISP), which launched in August 2025 to modernize how the FDA reviews imported products.
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FDA Increases Flexibility on Requirements for Cell and Gene Therapies to Advance Innovation

The U.S. Food and Drug Administration today announced it is sharing information about the agency’s flexible approach to overseeing chemistry, manufacturing and control (CMC) requirements for cell and gene therapies (CGT).
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FDA Issues Guidance on Modernizing Statistical Methods for Clinical Trials

The U.S. Food and Drug Administration today published draft guidance designed to facilitate the use of Bayesian methodologies in clinical trials of drugs and biologics, helping drug developers make better use of available data, conduct more efficient clinical trials, and deliver safe and effective t
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FDA Approves First Treatment for Children With Menkes Disease

The U.S. Food and Drug Administration today approved the Zycubo (copper histidinate) injection as the first treatment for Menkes disease in pediatric patients.