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How to Validate Computerized GxP Systems: Is Your Documentation Accurate, Comprehensive and Accessible?
Inadequate validation of electronic record keeping is a frequent citation in FDA 483s and warning letters, and the computer systems involved are critical for ensuring you have control over your processes.
If you have not previously carried out a computer system validation project, you may not be fully aware of the applicable regulatory requirements and how to define the scope of testing.
GxP computer systems that aren’t properly validated can lead to problems both internally — loss of critical data — and externally — regulatory action.
This presentation provides a step-by-step approach to the planning, execution and reporting of computer system validation activities. Validation documents are auditable records which are often reviewed during regulatory inspections. Therefore, it is important to not only perform testing that shows that the system functions as intended, but to adequately document the testing effort and the rationale used to determine the extent of testing. You will also receive tips on how to adequately manage testing resources to save time and money.
You will learn:
This course will be of benefit:
Chrysa Plagiannos, Senior Validation and Compliance Analyst at Montrium. Chrysa Plagiannos has 12 years’ experience in the pharmaceutical industry with extensive validation experience which includes the validation of manufacturing processes, equipment, facilities, and computerized systems. She also has experience in complaint management, investigation reporting and quality assurance functions. She has a degree in Chemical Engineering from McGill University.
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