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AHRMM25 Conference & Exhibition
Join us at AHRMM25 Conference & Exhibition, August 3-6 in Denver, Colorado for the leading event for health care supply chain.
House subcommittee holds hearing on cybersecurity vulnerabilities in legacy medical devices
The House Energy and Commerce Oversight and Investigations Subcommittee April 1 discussed cybersecurity threats in legacy medical devices during a hearing.
Court strikes down FDA rule on regulating lab-developed tests
The U.S. District Court for the Eastern District of Texas March 31 ruled that the Food and Drug Administration does not have the authority to regulate laboratory-developed tests.
Apply now for 2026 AHA Foster G. McGaw Prize
Health delivery organizations have until 1 p.m. ET May 6 to apply for the AHA’s 2026 Foster G. McGaw Prize, honoring organizations that demonstrate alignment between community health needs and co-designed programs.
AHA webpage highlights how hospitals and health systems integrate patient safety
As part of the AHA's Patient Safety Initiative, a dedicated webpage features case studies showing how hospitals and health systems across the nation are implementing effective and innovative programs to create a culture of safety, improve staff well-being and connect with their communities.
ICYMI: AHA podcast discusses the innovative design for Novant Health's Breast Center
In this recent episode of AHA’s Advancing Health podcast, Sara Robinson, senior associate healthcare architect at McMillan Pazdan Smith Architecture, and Jamie Feinour, vice president of operations at Novant Health Presbyterian Medical Center and president of Novant Health Charlotte Orthopedic Hospital, discuss how patient-centered design and innovative architecture come together to create spaces of healing for patients and providers, and how Sara's personal cancer journey impacted the design for Novant Health's Breast Center.
FDA issues final rule applying medical device rules to laboratory developed tests
The Food and Drug Administration April 29 issued a final rule that would phase out its general enforcement discretion approach for most laboratory developed tests over four years, citing concern that some of the tests may not provide accurate results or perform as well as FDA-approved in vitro diagnostic products.
SHSMD Awards and Recognition
News
Honoring health care's best and brightest, SHSMD recognize honorees for their outstanding achievements and contributions to the health care strategy and leadership community.
FDA recalls Medtronic Aortic Root Cannulas
The Food and Drug Administration has identified a Class I recall of Medtronic Aortic Root Cannulas due to a risk of unexpected loose material in the male luer used in the cannula.
Study finds social factors explain poorer cardiovascular health in rural areas
A study published March 31 by the Nationa