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Nelson Laboratories to Present Cleaning Validation Guidelines at BIOMEDevice San Jose
Date:11/20/2012

SALT LAKE CITY, Nov. 20, 2012 /PRNewswire/ -- Nelson Laboratories' (www.nelsonlabs.com) cleaning validation expert Alexa Tatarian will present "Cleaning Validations for Newly Manufactured Devices and Single Use Implants" to medical device manufacturers attending the 2012 BIOMEDevice San Jose Conference, Dec. 4-5 in San Jose, Calif. The presentation will take place at the Innovation Briefs Theater in booth #901 on Wednesday, Dec. 5 at 12:00 pm.

(Logo: http://photos.prnewswire.com/prnh/20120727/LA47745LOGO)

"Cleaning validations are an important step to prevent potentially dangerous devices from entering the market," said Tatarian, Nelson Laboratories chemistry department study director. "They are vital to ensure the overall surface cleanliness of newly manufactured devices and single use implants before they are distributed. Cleaning validations provide the data that manufacturers need on the overall cleanliness of their devices and implants before the products are market ready."

Although most medical device manufacturers know the importance of sending their product through standard sterility and biocompatibility testing before release, there are other ways a product can be contaminated during the manufacturing, production, cleaning and packaging of medical devices. Manufacturers who attend the Nelson Laboratories' Innovation Briefs presentation will learn the additional test options available to assess this contamination.

Watch a webinar on Cleaning Validations for Newly Manufactured Medical Devices and Single Use Implants: http://bit.ly/WbJDLX

"Our goal at BIOMEDevice San Jose is to provide medical device manufacturers with a guide for a test plan that gives them the cleanliness data they need to release their product on
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SOURCE Nelson Laboratories
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