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DTSTART:19700308T020000
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UID:2140535:Event:63138
DTSTAMP:20260523T210108Z
SUMMARY:Automating Laboratory Assays For the Bench
DESCRIPTION:This webinar on automating laboratory assays will teach yo
 u how to translate an assay that is performed manually to one that is 
 fully automated, with high quality and with proper validation and qual
 ity assurance for regulatory purposes.\n\nWhy Should You Attend:\nAuto
 mating laboratory assays from manual methods is rarely as simply as br
 inging in equipment, programming the assay in and letting it run. A ce
 rtain level of know-how is needed in order to understand the various p
 itfalls and issues that come with automating an assay.\nWith this webi
 nar, you will be able to understand the steps needed to transfer, vali
 date and maintain an automated assay in the laboratory. First, the ses
 sion will provide a key understanding of the various steps technicians
  perform on the bench, as certain methodologies are difficult to trans
 late onto automation. We will discuss how the procedure can be made to
  work on the automation in a way that is reliable and repeatable.\nWe 
 will cover the validation studies that must be performed and properly 
 scaled to make sure that the automation works reliably, and that any i
 ssues involving the method transfer have been properly resolved. Final
 ly, developing a quality assurance plan in concert with both the assay
  team and the manufacturer of the automation equipment will be discuss
 ed, as quality methods have to adapt to the new technology to maintain
  proper quality.\nAreas Covered in the Webinar:\nThe webinar will incl
 ude the following critical information you will need:\n\nWhat are the 
 individual steps needed to perform the assay on the bench?\nHow will y
 our assay adjust to your automation?\nWhat are the pitfalls to look ou
 t for during the method transfer process?\nHow scale up the assay vali
 dation of an automated system?\nHow to develop and manage the necessar
 y quality procedures with an automated system?\nHow to develop a quali
 ty plan to maintain the automated assay?\n\nWho will Benefit:\nThis to
 pic applies to personnel companies in the biotechnology and pharmaceut
 ical industry. The employees who will benefit most include:\n\nQuality
  Assurance\nResearch and Development\nBench Scientists\nLab Managers, 
 Directors\nMedical Technologists\nRegulatory Affairs\nValidation Speci
 alists\nMolecular Tester, Technologist, Supervisor\n\nInstructor Profi
 le:\nTodd Graham, is a masters-level bench scientist and medical tech
 nologist with a host of experience in both the clinical diagnostics an
 d biotechnology fields. He has work for a number of start-up firms in 
 the clinical diagnostics and biotechnology industries, as well as work
 ed for larger firms within both industries. He has a broad level of ex
 pertise in assay development for quality control, pharmaceutical devel
 opment and clinical diagnostics. His particular levels of expertise ar
 e molecular diagnostics, PCR, ELISA, quality control and training of b
 ench level personnel in clinical diagnostics and biotechnology.\n\nFor
  more information visit https://medtechiq.ning.com/events/automating-l
 aboratory-assays-for-the-bench
DTSTART;TZID=America/New_York:20140225T100000
DTEND;TZID=America/New_York:20140225T110000
CATEGORIES:medical
LOCATION:Online Event
WEBSITE:http://www.complianceonline.com/ecommerce/control/trainingFocu
 s/~product_id=703268?channel=medtechiq
URL:http://www.complianceonline.com/ecommerce/control/trainingFocus/~p
 roduct_id=703268?channel=medtechiq
CONTACT:+1-650-620-3915
ORGANIZER:ComplianceOnline
ATTACH;FMTTYPE="image/jpeg":http://storage.ning.com/topology/rest/1.0/
 file/get/2562006613?profile=original
ATTENDEE;ROLE=REQ-PARTICIPANT;PARTSTAT=ACCEPTED;RSVP=TRUE;CN=Complianc
 eOnline:https://medtechiq.ning.com/profile/Referral512
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