MEDICAL DEVICES 2011 - You have a sterility or Bioburden test failure

Website http://complianceonline.com/ecommerce/control/trainingFocus/~product_id=701503?channel=ourglocal | Edit Freely

Category Medical Devices,conference,event,Webinar

Deadline: April 28, 2011 | Date: April 28, 2011

Venue/Country: Palo Alto, U.S.A

Updated: 2011-03-11 18:55:20 (GMT+9)

Call For Papers - CFP

All sterile products require some level of sterility and bioburden testing during validation and then during routine production. What actions your company takes when this testing exhibits results that do not meet specifications can be critical from a regulatory and safety standpoint. You need to know what and how to investigate during these potential failures or out-of-specification conditions to identify the root cause. You also need to know if the failure impacts product release, do you need to recall product, is your validation okay, and are there any actions that can be taken to prove there is no product impact.

NOTE: Use This Promocode ( 117660 ) To Get 10% Discount.