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DTSTART:19700308T020000
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DTSTAMP:20260416T130607Z
SUMMARY:CGMP controlled Raw Materials
DESCRIPTION:This webinar will help the attendee gain an understanding 
 of the appropriate way to design the processing of all cGMP Controlle
 d raw materials that are used for the manufacturing of drug product. 
 The scope of this webinar applies to all cGMP controlled raw materials
  that are received, requiring testing, release and issuance of specifi
 cations. It also applies to the processing of changes and retiring of 
 previously issued controlled raw materials specification within the pr
 oduct manufacturing process. cGMP Raw materials that are used for prod
 uct manufacturing has to be released for use in the production process
 . Guidance will be given as to the steps that every drug product manuf
 acturer should follow in order to process all incoming cGMP controlled
  raw materials which includes the release for use in the manufacturing
  of products.\nWhy Should You Attend:\nThis webinar will provide such 
 guidance as to the process of ensuring that there all the steps are fo
 llowed to avoid producing an adulterated product as defined by the 21 
 CFR 110.80 Processes and Controls. This webinar will provide a great r
 esource to Pharmaceutical, Biotechnology and Medical Device Industries
  personnel that will like to have a clear understanding of the Designi
 ng the Receipt, Handling and Processing, Specification, Inventory Trac
 king, and Qualification of a cGMP Controlled Raw Materials.\n\nAreas C
 overed in the Webinar:\n\nRegulatory Requirements for all Incoming cGM
 P Controlled Raw Materials:\nWhat does the regulation say about raw ma
 terials that are received for cGMP use\n\n\nReceipt and Storage of cGM
 P Controlled Raw Materials\nDelineation of Raw Materials\nCritical\nNo
 n-critical\n\n\nAcceptable Storage of cGMP Controlled Raw Materials\nC
 ontrol of Conditions (Temperature and Humidity Control)\nControl of Lo
 cation (Lock and Key)\nQuarantine, Segregation and Labeling Requiremen
 ts\nTesting and Qualification\nApproval and Release for use\nDispositi
 on and Release for Use Requirements\nDispensing and Traceability (Trac
 king)\n\n\n\n\n\nWho Will Benefit:\nThis topic applies to personnel/co
 mpanies in the Pharmaceutical, Biotechnology and Medical Device Indust
 ries. The employees who will benefit most include:\n\nQuality Control 
 Analysts and Management\nSenior Management\nManufacturing Associates a
 nd Management\nShipping, Receiving, Warehouse Personnel and Management
 \nRaw Material Receipt and Testing Personnel\n\n\n\nFor more informati
 on visit https://medtechiq.ning.com/events/cgmp-controlled-raw-materia
 ls
DTSTART;TZID=America/New_York:20211116T100000
DTEND;TZID=America/New_York:20211116T130000
CATEGORIES:webinar
LOCATION:online
WEBSITE:https://www.complianceonline.com/qualification-of-cgmp-control
 led-raw-materials-webinar-training-705148-prdw?channel=MedTech%20I.Q
URL:https://www.complianceonline.com/qualification-of-cgmp-controlled-
 raw-materials-webinar-training-705148-prdw?channel=MedTech%20I.Q
CONTACT:8887172436
ORGANIZER;CN=ComplianceOnline:https://medtechiq.ning.com/profile/Refer
 ral512
ATTACH;FMTTYPE="image/jpeg":
ATTENDEE;ROLE=REQ-PARTICIPANT;PARTSTAT=ACCEPTED;RSVP=TRUE;CN=Complianc
 eOnline:https://medtechiq.ning.com/profile/Referral512
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