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DTSTART:19700308T020000
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UID:2140535:Event:68880
DTSTAMP:20260520T052346Z
SUMMARY:Webinar on Process Robustness - The New FDA Paradigm
DESCRIPTION:Description :\nProcess robustness is not a new concept; ho
 wever, it may be new to organizations that are not required to perform
  validation. There is more to a robust process than having a dosage fo
 rm pass final specifications. Robustness cannot be tested into a produ
 ct; rather, it must be incorporated into the design and development of
  the product.\nThis training is the first step in understanding how th
 e performance of the product and process can be monitored to ensure ro
 bustness can be maintained. The training will discuss key concepts wit
 h process robustness, defines common terms, details a methodical appro
 ach to robust process development, and discusses tools and metrics tha
 t can be used during development or for ongoing process monitoring.\nA
 reas Covered in the Session :\nKey concepts associated with Process Ro
 bustness\nDefines common terms\nDetails a methodical approach to robus
 t process development\nTools and metrics\nWho Will Benefit:\nQuality D
 irectors and Sr. Directors\nQA Specialists (Senior Level)\nCompliance 
 Departments\nQuality System Consultants\nProduction Management Teams\n
 Technical Services Manager\nOperations Departments\nProcess Engineers\
 n\nFor more information visit https://medtechiq.ning.com/events/webina
 r-on-process-robustness-the-new-fda-paradigm
DTSTART;TZID=America/New_York:20160412T130000
DTEND;TZID=America/New_York:20160412T140000
CATEGORIES:webinar
LOCATION:Online
WEBSITE:https://compliancetrainings.com/SiteEngine/ProductDetailView.a
 spx?id=FDB1813
URL:https://compliancetrainings.com/SiteEngine/ProductDetailView.aspx?
 id=FDB1813
CONTACT:4169154458
ORGANIZER:Compliance Trainings
ATTACH;FMTTYPE="image/jpeg":
ATTENDEE;ROLE=REQ-PARTICIPANT;PARTSTAT=ACCEPTED;RSVP=TRUE;CN=complianc
 etrainings:https://medtechiq.ning.com/profile/compliancetrainings
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