
Feature|Videos|October 21, 2025
When Did the FDA Begin Regulating UVC Devices in Healthcare Environments?
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Hospitals are embracing whole-room microbial reduction as a backstop to inconsistent surface cleaning, and the FDA has now created a formal regulatory pathway that finally defines what compliance and validated claims look like. That clarity raises new questions for infection prevention and environmental services teams about procurement, risk management, and how these tools fit into patient-safety strategies. In this section, our panelists explain how we got here and what the new oversight means for real-world adoption and outcomes.
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This week's coverage in Infection Control Today centered on a common thread: the systems, partnerships, and data that let infection prevention teams catch problems before patients are harmed.

UPMC’s genomic surveillance initiative earned national recognition for patient safety. Alexander Sundermann, DrPH, CIC, FAPIC, AL-CIP, explains how the award could help infection preventionists secure leadership support and sustainable funding for earlier outbreak detection.

Knowing the protocol is only the beginning. In The Clean Bite, Sherrie Busby explores how explaining the why, addressing staff concerns, and creating clear procedures can help dental teams make infection control part of everyday practice.

What might infection prevention rounds miss when visible conditions dominate the conversation? Tommy Davis, PhD, CMIP, a member of ICT's executive advisory board, makes the case for structured observations of clinical workflows, shared accountability, and greater attention to environmental services staff’s insights.

A proposed $27.7 million reduction in AHRQ funding raises questions about support for infection prevention research and implementation. Here is what the September 25 announcement identifies, as well as what remains unknown about specific IPC programs.

Two posters presented by Karen Jones, MPH, RN, CIC, FAPIC, at the APIC Annual Conference and Exposition examine surveillance responsibilities and staffing in small hospitals, as well as IPs’ reported experiences after implementing electronic surveillance. Findings highlight opportunities for more investigation, rounding, and communication.

A followed procedure can still leave patients at risk if it no longer matches validated requirements. Annetta L. McKnight, MHA, BSN, CRCST, CER, examines how infection prevention and sterile processing can identify process drift, assess disruptions, and strengthen shared oversight of medical device reprocessing.
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