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LAST-MODIFIED:20260912T221527Z
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DTSTAMP:20261008T033429Z
DTSTART;TZID=Europe/London:20250220T090000
DTEND;TZID=Europe/London:20250220T100000
SUMMARY:GoToWebinar - Effective Cleanroom Monitoring in Sterile Pharmaceu
 tical Plants
LOCATION:GoToWebinar - See conference call information below
UID:72e934ee-a25e-4aa0-9817-d87e02d37d0f@goto.com
ORGANIZER:emeamarketing@golighthouse.com
DESCRIPTION:1. Click and join at the specified time and date:\nhttps://gl
 obal.gotowebinar.com/join/7518197072729707615/172870610\nNote: This link
  should not be shared with others\; it is unique to you.\n\n2. Call in u
 sing the phone number(s) below:\n\nNo audio information found\n\n\nIn th
 is webinar\, you will gain insights into the key aspects of cleanroom mo
 nitoring in sterile pharmaceutical plants\, with a special focus on viab
 le and non-viable particle monitoring. We will provide a decision tree f
 or determining the critical factors in cleanroom monitoring and discuss 
 best practices for achieving compliance.\n\nYou will find answers to the
  following topics\;\n• Cleanroom Monitoring Systems for Sterile Environm
 ents \n• How to enhance the accuracy of sample data in sterile pharmaceu
 tical plants \n• Common weaknesses in particle counters used in sterile 
 environments \n• Importance of good housekeeping for particle counters \
 n• Efficiency of particle sampling in sterile environments \n• Utilizing
  the decision tree for effective monitoring – with practical examples \n
 • Understanding and mitigating particle losses during monitoring \n• Mon
 itoring critical locations and utilizing risk assessments effectively \n
 • The role of Isokinetic Sampling and sample tubing flow paths \n• Data 
 integrity and its importance in sterile environments\n\nWho Should Atten
 d?\n• Pharmaceutical cleanroom professionals \n• Cleanroom Validation an
 d Qualification Experts \n• Production specialists \n• Cleanroom design 
 engineers \n• Risk assessment teams \n• Cleanroom operators \n• Contamin
 ation control specialists \n• Environmental Monitoring Plan execution te
 am members \n• Engineering professionals \n• QA/QC Specialists\n\n
X-ALT-DESC;FMTTYPE=text/html:<HTML><HEAD><TITLE></TITLE><BODY><FONT SIZE=
 2><b>1. Click and join at the specified time and date:</b></FONT><BR><FO
 NT SIZE=2>https://global.gotowebinar.com/join/7518197072729707615/172870
 610</FONT><BR><FONT SIZE=2>Note: This link should not be shared with oth
 ers\; it is unique to you.</FONT><BR><BR><FONT SIZE=2><FONT SIZE=2><b>2.
  Call in using the phone number(s) below:</b></FONT><BR><BR><BR><FONT SI
 ZE=2>No audio information found</FONT><BR></BODY></HTML></FONT><BR><FONT
  SIZE=2>In this webinar\, you will gain insights into the key aspects of
  cleanroom monitoring in sterile pharmaceutical plants\, with a special 
 focus on viable and non-viable particle monitoring. We will provide a de
 cision tree for determining the critical factors in cleanroom monitoring
  and discuss best practices for achieving compliance.\n\nYou will find a
 nswers to the following topics\;\n• Cleanroom Monitoring Systems for Ste
 rile Environments \n• How to enhance the accuracy of sample data in ster
 ile pharmaceutical plants \n• Common weaknesses in particle counters use
 d in sterile environments \n• Importance of good housekeeping for partic
 le counters \n• Efficiency of particle sampling in sterile environments 
 \n• Utilizing the decision tree for effective monitoring – with practica
 l examples \n• Understanding and mitigating particle losses during monit
 oring \n• Monitoring critical locations and utilizing risk assessments e
 ffectively \n• The role of Isokinetic Sampling and sample tubing flow pa
 ths \n• Data integrity and its importance in sterile environments\n\nWho
  Should Attend?\n• Pharmaceutical cleanroom professionals \n• Cleanroom 
 Validation and Qualification Experts \n• Production specialists \n• Clea
 nroom design engineers \n• Risk assessment teams \n• Cleanroom operators
  \n• Contamination control specialists \n• Environmental Monitoring Plan
  execution team members \n• Engineering professionals \n• QA/QC Speciali
 sts\n</FONT><BR></BODY></HTML>
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