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From GlobalCompliancePanel
Efficient Computer System Validation - GlobalCompliancePanel
Overview: This webinar details all of the templates used to create validation documentation, usually saving two-thirds of the time and costs. The 10-step risk-based approach to COTS software validation minimized documentation and ensures efficient implementation of new and upgraded computer systems. This experience will prepare you to perform a validation project.
Tuesday, May 15, 2012
10:
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Efficient Computer System Validation - 10 Easy Steps - Webinar By GlobalCompliancePanel
..., usually saving two-thirds of the time and costs.
The 10-step risk-based approach to COTS software validation minimized documentation and ensures efficient implementation of new and upgraded computer systems. This experience will prepare you to perform a validation project.
Areas Covered in the Session:
* Learn which documents the FDA expects to audit.
* How to use the
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21 CFR Part 11 - Compliance for Electronic Records and Signatures - Webinar by GlobalCompliancePanel
This webinar details the regulation and how it applies to computerized systems.
Learn exactly what is needed to be compliant for all three primary areas: SOPs for the IT infrastructure, industry standards for software product features, and the 10-step risk-based validation approach. This webinar demystifies Part 11, and get you on the right track for using electronic records and signatures to
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21 CFR Part 11 - What you need to know to pass the new FDA audits - Webinar by GlobalCompliancePanel
This webinar details the regulation and how it applies to computerized systems.
Learn exactly what is needed to be compliant for all three primary areas: SOPs for the IT infrastructure, industry standards for software product features, and the 10-step risk-based validation approach. This webinar demystifies Part 11, and get you on the right track for using electronic records and signatures to
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Ten-Step Process for COTS Computer System Validation - Reduce Time and Cost
GlobalCompliancePanel brings a new webinar on the topic of Ten-Step Process for COTS Computer System Validation - Reduce Time and Cost.
Webinar will be on April 6, 2010. Webinar will be presented by David Nettleton.
This webinar details all of the templates used to create validation documentation, usually saving two-thirds of the time and costs. The 10-step risk-based approach to COTS software
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From Global BioPharmaceutical Resources, Inc. (GBPR, Inc.)
21 CFR Part 11 the details of what it means
This webinar takes the requirements of Part 11 and details them into specific things to do in all three primary areas: SOPs, product features, and validation. It describes what to do to be compliant thereby avoiding 483s and warning letters. All required IT SOPs are covered. All industry standards product features are discussed. The 10-step risk-based validation approach is outlined so that the
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COTS Software Validation 10 Easy Steps
... efficient techniques for performing COTS validation. The 10-step risk-based approach to COTS software validation makes documentation more manageable and understandable. Learn how to increase productivity and minimize resources, usually saving two-thirds of the time and costs. Ensuring compliance of new and upgraded computer systems. Learn how to use risk management to improve system
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