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DTSTART:19700308T020000
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UID:2140535:Event:470963
DTSTAMP:20260525T043441Z
SUMMARY:Basic Cleanroom Technology, Operation and Contamination Contro
 l in a Nutshell
DESCRIPTION:Attend this webinar to understand the Clean Room regulatio
 ns, design, classification, sources and types of particles. Learn how 
 to create a common ground between these varying regulations and requir
 ements. It will discuss the types of micro-organisms, routine monitori
 ng processes, and typical mitigation steps to effective contamination 
 control.\n\nWhy Should You Attend:\nThis 90-minute accredited training
  will offer a basic understanding of the Clean Room regulations, desig
 n, classification, sources and types of particles. The different class
 ifications and limits for Clean room particles as it applies to variou
 s regulatory bodies’ and requirements (US, EU and ISO) will be addre
 ssed. Special attention will be given to understanding how to create a
  common ground between these varying regulations and requirements will
  be discussed. The types of micro-organisms, routine monitoring proces
 ses, typical mitigation steps in ensuring an effective contamination c
 ontrol through monitoring, sanitization, cleaning, personnel training,
  gowning, and material, product and personnel flow during a clean room
  operation will be addressed.\n\nLearning Objectives:\n\nDiscuss the b
 asics, background and types of clean room classification.\nDescribed s
 ources of clean room contamination, settling rates and contamination c
 ontrol process.\nList the various classifications/levels, regulations,
  and clean room applications based on classification.\nDescribe clean 
 room validation process and rationale for performing the validation pr
 ocess.\nDiscuss the routine clean room monitoring processes and invest
 igations associated with a clean room monitoring excursion.\n\n\nAreas
  Covered in the Webinar:\nModule#1 (Basics, Background and Clean room 
 Classification)\n\nSummary of the Regulations Guiding Clean room Techn
 ology, Design and Verification\nTypes of Clean room Classifications an
 d Requirements\nEU Requirements and Classification\nUSP Requirements a
 nd Classification\nISO Requirements and Classification\nBridging the G
 ap between the various Regulatory Bodies’ and Requirements\n\n\nType
 s and Sizes of Clean room Particles\n\nWho Will Benefit:\nThis webinar
  will provide a great resource to personnel involved within the follow
 ing departments in the Pharmaceutical, Biotechnology, Diagnostics, Dru
 gs, Cell Therapy, Biologics and Medical Device industries:\n\nQuality 
 Control\nManufacturing/Production\nSenior Management\nRegulatory Affai
 rs\nQuality Assurance\nCompliance\nDesign Engineers\nFacility, Mainten
 ance and Engineering\nTest Contractors\n\nHowever, if you are already 
 familiar with how to achieve an effective Clean room technology and co
 ntamination control, you may recommend this webinar to anyone in your 
 company that may require additional knowledge about this subject.\n\nF
 or more information visit https://medtechiq.ning.com/events/basic-clea
 nroom-technology-operation-and-contamination-control-in
DTSTART;TZID=America/New_York:20220208T100000
DTEND;TZID=America/New_York:20220208T130000
CATEGORIES:webinar
LOCATION:online
WEBSITE:https://www.complianceonline.com/cleanroom-technology-operatio
 n-contamination-control-webinar-training-706142-prdw?channel=MedTech%2
 0I.Q
URL:https://www.complianceonline.com/cleanroom-technology-operation-co
 ntamination-control-webinar-training-706142-prdw?channel=MedTech%20I.Q
CONTACT:8887172436
ORGANIZER:Complianceonline
ATTACH;FMTTYPE="image/jpeg":https://storage.ning.com/topology/rest/1.0
 /file/get/10043741672?profile=original
ATTENDEE;ROLE=REQ-PARTICIPANT;PARTSTAT=ACCEPTED;RSVP=TRUE;CN=Complianc
 eOnline:https://medtechiq.ning.com/profile/Referral512
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