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You have a Sterility Failure or Bioburden Excursion - Now What?
ComplianceOnline
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2:00 AM
$249.00
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Compliance training on Sterility or Bioburden test failures, items to be investigated to determine the root cause and the follow up to the investigation.
ComplianceOnline
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2:00 AM
$249.00
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Tags:
analysis, bioburden, compliance, ComplianceOnline, failure, failures, investigations, News, process, RCA, root, sterility, Sterilization, test, training, validation
03/08/2013
2:00 AM
2:00 AM
1
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Reducing Ethylene Oxide (EO) Sterilization Costs While Maintaining Regulatory...
ComplianceOnline
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5:00 PM
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Instructor: Marisel Ortiz In this Ethylene Oxide (EO) Sterilization training, you will learn how to evaluate your sterilization process for cost reduction/process efficiency, and also...
ComplianceOnline
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5:00 PM
Free
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Compliance, ComplianceOnline, Costs, Ethylene, Maintaining, News, Oxide, Reducing, Regulatory, Sterilization
08/31/2012
5:00 PM
5:00 PM
2
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2-day In-person Seminar: Medical Device Sterilization: Corrective & Preventiv...
ComplianceOnline
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4:00 PM
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The course will begin with an overview of EO sterilization, explaining which aspects of the process often cause confusion
ComplianceOnline
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4:00 PM
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application, CAPA, ComplianceOnline, device, Medical, News, process, seminar, sterilization, validation
06/14/2012
4:00 PM
4:00 PM
6
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Hotel chain rolls out UV sterilization
Out of sight, out of mind. That's a mantra hotel guests tend to adopt as they tuck into rooms inhabited by hundreds of previous guests -- and possibly the microscopic germs and debris...
05/31/2012
11:36 PM
11:36 PM
7
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You have a Sterility Failure or Bioburden Excursion
Webinar Hero
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5:00 PM
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This Sterility or Bioburden test Webinar/training will discuss on various items that should be investigated to determine the root cause and the follow up to the investigation.
Why Should...
Webinar Hero
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5:00 PM
Free
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analysis, bioburden, compliance, failure, failures, Hero, investigations, RCA, root, sterility, Sterilization, test, training, Webinar
04/04/2012
5:00 PM
5:00 PM
7
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Application of CAPA to the Device Sterilization Process
Webinar Hero
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4:00 PM
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Do you use a Contract Sterilizer for your medical device sterilization? Are you not an expert in industrial sterilization? If you answered “yes” to either of these questions, this seminar...
Webinar Hero
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4:00 PM
Free
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CAPA, Compliance, Device, Hero, Online, pplication, Process, Seminar, Sterilization, Training, Webinar
03/14/2012
4:00 PM
4:00 PM
3
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Submission Documentation for Sterilization Process Validation - A Comprehensi...
ComplianceOnline
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6:00 PM
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Instructor: Colin Davis In this sterility assurance documentation webinar, you will learn specifically what information is required in sterility assurance documentation for injectable...
ComplianceOnline
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6:00 PM
Free
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Tags:
Approvable, CMC, ComplianceOnline, Comprehensive, Content, Documentation, News, Process, Sterilization, Submission, Validation, View
02/23/2012
6:00 PM
6:00 PM
9
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Submission Documentation for Sterilization Process Validation
Webinar Hero
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5:00 PM
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In this sterility assurance documentation webinar, you will learn specifically what information is required in sterility assurance documentation for injectable drug products and how to...
Webinar Hero
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5:00 PM
Free
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Tags:
aseptic, assurance, CMC, content, CTD, documentation, format, Hero, Process, processes, sterility, Sterilization, Submission, terminal, Validation, Webinar
02/23/2012
5:00 PM
5:00 PM
8
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Application of CAPA in (Device) Sterilization – For the Non-Expert
Webinar Hero
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3:30 PM
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This webinar will review the typical non-conformances experienced in the (Medical Device) sterilization process and the course of action that should be taken by the manufacturer or...
Webinar Hero
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3:30 PM
Free
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action, Application, assurance, basics, CAPA, corrective, deficiencies, Device, Hero, Medical, process, Radiation, Sterilization, Webinar
01/20/2012
3:30 PM
3:30 PM
5
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Testing considerations for sterilization validation and routine sterilization...
Instructor: Gerry O Dell This sterilization validation process training webinar will review the FDA or ISO requirements for tests following validation and emphasis is placed on the...
10/21/2011
5:00 PM
5:00 PM
