Reusable medical devices (such as surgical tools, etc.) need to be cleaned and/or sterilized before each use.  To ensure this is the case, manufacturers are required to validate their cleaning/sterilization instructions accordingly.  This webinar aims to address a range of factors to consider when developing such protocols.

Topics covered included:

• Categories of medical devices
• Intended use of device
• Experimental design
• Testing considerations
• Worst-case testing
• Test soils
• Cleaning
• Disinfection
• Sterilization.

This webinar recording will be of interest to medical device manufacturers who wish to progress 510(k) submissions to the FDA or submissions to other regulatory authorities.

Registered users can view the recording. Registration is simple, free and quick.