Recent outbreaks of deadly infections linked to flexible endoscopes have made headlines, and the Food and Drug Administration has issued strict guidelines for reprocessing these devices.
Welcome to OR Manager, your source of information and insight into the clinical and business management of the surgical suite. This article is only available to OR Manager subscribers. To read this article, and gain access to all OR Manager resources, please log in below:
Username
Password
Explore Subscription Options
Please contact our Customer Service Team if you are unable to log in at clientservices@accessintel.com or 1-888-707-5814.
It is with great excitement that we welcome you to…
Find out more
As you dive into this year's OR Manager Conference, here…
What happens when a veteran perioperative leader walks away from…