Any and all steps taken by you and your staff to reduce the risk of an instrument contaminated with organic debris being returned to surgery will help reduce the risk of a patient contracting...
The No. 1 responsibility of everyone involved in reusable medical device reprocessing is to minimize the risk of patient harm caused by a device that remains contaminated with organic debris...
America has entered a whole new phase of the COVID-19 pandemic. As of January 8, 2021, over 2 million U.S. citizens have been vaccinated with the Pfizer/BioNTech’s vaccine or with...
On Friday, December 18, 2020 the U.S. Food and Drug Administration (FDA) issued an emergency use authorization (EUA) for a second vaccine for the prevention of COVID-19 to Moderna. This...
On Friday, November 20, 2020, Pfizer and BioNTech submitted a request to the US Food and Drug Administration (FDA) for emergency use authorization for their coronavirus vaccine candidate. This request...
