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DTSTAMP:20260523T141432Z
SUMMARY:Webinar On \"Laboratory Controls – In the Quality System Env
 ironment\"
DESCRIPTION:\nDescription :\nAlthough the pharmaceutical industry is o
 perating under a regulation written in the mid 1970s, there has been a
  considerable change in technology and the FDA has released a number o
 f guidance documents that impact what is considered to be compliance. 
 In this webinar we will discuss laboratory controls expected by the re
 gulators and consistent with recent guidance and industry practice.Obj
 ective\nThe objective of this webinar is to inform and educate individ
 uals who work in, manage, audit and review documents generated by Qual
 ity Control Laboratories and .Analytical Development Laboratories abou
 t systems that should be in place to support contemporary Quality Syst
 ems.\n\n\n\n\nAreas Covered in the Session :\n\nTrending\nOOS investig
 ations\nTest procedures\nAnalytical method validation\nTest method unc
 ertainty\nInstrument qualification and calibration\nQuality Metrics in
  the Laboratory\n\n\n\n\n\nWho Will Benefit:\n\nManagers\nSupervisors\
 nAnalysts working the Quality Control\nAnalytical Development Laborato
 ries\nQuality Assurance Laboratory Document Reviewers\nQuality Assuran
 ce Auditors\n\n\n\n\n\nAbout Speaker:\nJohn G. (Jerry) Lanese is an in
 dependent consultant with a focus on Quality Systems and the component
 s of an effective Quality System. He received a BA and MS from Middleb
 ury College and a Ph.D. in Analytical Chemistry from the University of
  Michigan and began his career teaching Analytical Chemistry in a smal
 l liberal arts college. Dr. Lanese moved from the academic environment
  to the pharmaceutical industry where he has managed Analytical Resear
 ch, Quality Control and Quality Assurance functions.  In 1994 Dr. Lane
 se formed his own company, The Lanese Group, and since that time he ha
 s been a consultant in the area of quality system and cGMP compliance 
 and has audited and consulted with small and large medical device and 
 pharmaceutical companies, including companies under FDA Consent Decree
 , API and excipient manufacturers, electronic firms and other manufact
 uring organizations.\n\n\n\n\n\n\nFor more information visit https://m
 edtechiq.ning.com/events/webinar-on-laboratory-controls-in-the-quality
 -system-environment
DTSTART;TZID=America/New_York:20180328T130000
DTEND;TZID=America/New_York:20180328T143000
CATEGORIES:online, "/", webinar
LOCATION:Online
WEBSITE:https://www.compliancetrainingpanel.com/Webinar/Topic?WB=MD000
 87
URL:https://www.compliancetrainingpanel.com/Webinar/Topic?WB=MD00087
CONTACT:1-844-216-5230
ORGANIZER:Compliance Training Panel (Sam Miller)
ATTACH;FMTTYPE="image/jpeg":http://storage.ning.com/topology/rest/1.0/
 file/get/2562016428?profile=original
ATTENDEE;ROLE=REQ-PARTICIPANT;PARTSTAT=ACCEPTED;RSVP=TRUE;CN="Sam Mill
 er":https://medtechiq.ning.com/profile/SamMiller
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