Cleaning Validation of Reusable Medical Devices

Webinar Recording

Presented by Dr Craig Donald, the webinar discusses reusable medical devices (such as surgical tools, etc.) which need to be cleaned and/or sterilized before each use. Manufacturers are required to validate their cleaning/sterilization instructions accordingly. The webinar addresses a range of factors to consider when developing such protocols.

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.

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