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DESCRIPTION:This training will review the best practices establishing and 
 conducting a cleaning validation for reusable medical devices. It will al
 so address the requirements of ANSI/AAMI ST 98.\n\nWhy Should You Attend:
 \n\nReusable medical devices continue to receive scrutiny from regulatory
  agencies both in the United States and internationally. Since the advent
  of&nbsp\;ANSI/AAMI ST 98&nbsp\;there has been more clarity in how to per
 form these validations but it is still important to know the regulatory e
 xpectations to reduce the likelihood that submissions will not be accepte
 d and require additional testing or worst case that the testing needs to 
 be repeated.\n\nThis presentation will address the most current expectati
 ons for cleaning validations of reusable medical devices that are perform
 ed in support of the instructions in the instruction for use (IFU). It wi
 ll include both manual and automated cleaning processes as well as inform
 ation on how to choose test soils\, markers for challenging cleaning\, an
 d the acceptance criteria to use to establish effective cleaning.\n\nArea
 s Covered in the Webinar:\n\n\nCleaning validation design - automated cle
 aning.\nCleaning validation design - manual cleaning\nIFU information to 
 be supported.\nChoosing test soils.\nChoosing markers.\nExpectations for 
 controls.\nAcceptance criteria selection.\nReport preparation.\n\nWho Wil
 l Benefit:\n\nThis webinar will provide valuable information to all compa
 nies that manufacture reusable medical devices in environments:\n\n\nQA p
 ersonnel\nValidation specialists\nRegulatory\nR&amp\;D\n
DTEND:20250210T113000
DTSTAMP:20260514T153457Z
DTSTART:20250210T100000
LOCATION:\,
SEQUENCE:0
SUMMARY:This training will review the best practices establishing and cond
 ucting a cleaning validation for reusable medical devices. It will also a
 ddress t...
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