News

Creating Adequate Reprocessing Instructions

Reusable Medical Device manufacturers are required by the US Food and Drug Administration to validate their reprocessing instructions. Statistics say, about one in 25 hospital patients has at least one healthcare-associated infection. With adequate reprocessing instructions, we can help reduce these statistics!

Posted on: September 7, 2017

Categories: News and White Paper

Tags: Cleaning Validation and Reusable Device