Efficient Computer System Validation – 10 Easy Steps – Webinar By GlobalCompliancePanel
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.
Areas Covered in the Session:
- Learn which documents the FDA expects to audit.
- How to use the risk-based validation approach to lower costs.
- How to link requirements, specifications, risk management, and testing.
- Document a computer system validation project using easy to understand fill-in-the-blank templates.
- Based on: “Risk-Based Software Validation – Ten Easy Steps” (Davis Horwood International and PDA – www.pda.org, 2006).
- Step-by-step instructions for performing and documenting a risk assessment, and how to use the results to reduce validation documentation.
- Reduce testing by writing test cases that trace to elements of risk management.
Who Will Benefit:
- IT
- QA
- QC
- Laboratory staff
- Managers
- GMP, GCP, GLP professionals
Price List:
10:00 AM PST | 01:00 PM EST
Issued By: globalpanel
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GlobalCompliancePanel is an online training gateway delivering high quality regulatory & compliance trainings in a simple, cost effective and in a user friendly format. GlobalCompliancePanel offers a broad range of channels for broadcasting and exchange of information through web based training, web alerts & discussion forums
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