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.

Areas Covered In the Session: Key points regarding protocol development A summary of standards Key tests to be familiar with Expected results Packaging issues Labeling issues Who will benefit: Engineering Quality Validation Microbiology Process/ Scientist Manufacturing Regulatory Affairs

Price List: Live : $245.00 Corporate live : $995.00 Recorded : $295.00

webinars@globalcompliancepanel.com http://www.globalcompliancepanel.com

Phone: 800-447-9407 Fax: 302-288-6884

Dates: Wednesday, February 22, 2012

Location: Online Training, Delaware, United States