Computer System Validation

6 years ago Posted By : User Ref No: WURUR25204 0
  • Image
  • TypeWebinar
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  • Location Baltimore, Maryland, United States
  • Price
  • Date 19-09-2018
Computer System Validation, Baltimore, Maryland, United States
Webinar Title
Computer System Validation
Event Type
Webinar
Webinar Date
19-09-2018
Last Date for Applying
19-09-2018
Location
Baltimore, Maryland, United States
Organization Name / Organize By
ComplianeTrainingpanel
Organizing/Related Departments
R&D
Organization Type
Event Organizing Company
WebinarCategory
Technical
WebinarLevel
International
Related Industries

Education/Teaching/Training/Development

Communications

Location
Baltimore, Maryland, United States

FDA requires that all software in computer systems used in GxP activities must be validated. Validation of computer system software is completely different than validation of device software (embedded software). Validation is more than testing. It is testing plus design control and configuration management.

How to plan and conduct a risk based validation will be explained. Overall risk for computer system is a combination of software complexity and product risk as determined by probability, severity and detectability rankings. Also involved in the risk evaluation is the requirement for purchased software supplier qualification. You’ll learn how to integrate risk based supplier evaluation into the validation process.

Validation Master plan and System Validation Plans will be explained

Testing, based on risk, includes requirements validation and IQ, OQ and PQ. A procedure for each level of complexity and risk will be described.

Why ?

Validation of computer system software is completely different than validation of device software (embedded software). Attempting to conduct a CSV following device software validation concepts could result in a 483 or rejection of a product approval submission.

You will learn in detail:

  • Validation life cycle models and Validation Plan contents
  • How to determine the complexity category of your system based on GAMP 5 principles
  • How to evaluate risk level using GAMP 5 modifications to the ISO 14971 procedure
  • What level of testing is necessary based on software complexity and risk
  • Integrating software supplier evaluation into the validation process
  • What requirements documentation is necessary
  • How to plan and conduct IQ, OQ and PQ

Areas Covered in the Session :

  • Validation strategy
  • Requirements documentation
  • Complexity and risk analysis
  • Creating a detailed test plan based on risk
  • Supplier qualification
  • IQ, OQ and PQ

Who Will Benefit:

  • Computer system developers
  • Systems development engineers
  • QA/ QC
  • Lab Managers and Analysts
  • Production Managers
  • Engineering managers

Others Details

Venue: Online Speaker Name: Edwin Waldbusser Price : $ 229 Wednesday, September 19, 2018  EST 13:00 Duration : 60 Minutes Tel: +1-844-216-5230 www.compliancetrainingpanel.com

Registration Fees
Available
Registration Fees Details
Price : $ 229
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  Online  Pin/Zip Code : 20817
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