Sponsor or Organizer: Global Compliance Panel
Description: Validation of reusable medical devices requires that the manufacturer develop methods for cleaning (after use) washing to remove all foreign matter possibly disinfecting and repackaging for the next use.The diversity of medical devices their intended use and classification in accordance with the food and drug administration requires that the manufacturer develop and validate the reprocessing of the medical device.
Who will benefit: Engineering Quality Validation Microbiology Process/ Scientist Manufacturing Regulatory Affairs
Price List: Live : $245.00 Corporate live : $995.00 Recorded : $295.00
Dates: Wednesday, February 22, 2012
Location:
Online Training, Delaware, United States
|