Cleaning, disinfection, and sterilization – what is in between?

Since the release of the FDA guidance on reprocessing, reusable medical devices have taken a huge place in FDA approvals. Reprocessing validations are challenging and could delay or derail the entire device approval. The presentation will provide an overview of this guidance and will help manufacturers to handle these requirements, ensuring compliance with the most recent FDA expectations.

this lecture is presented by

Nicola Revellin | Senior Medical Research Scientist|  NAMSA