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This procedure provides detailed outlines of what needs to be included in the most important computer system validation deliverables, including requirements, validation plans, IQ, OQ and PQ protocols, protocol reports, and the validation final report. This procedure is of great value to those who are not familiar with these types of documents and those who want to verify that what they are including in their documents is what auditors look for. 20 pages
Provider: BPA
Shipping: Available for download - Link will be provided in My ComplianceOnline section
Price: $99.00

Product Detail:
  • This procedure applies to all computer system validation plans, protocols (IQ, OQ, or PQ), protocol reports , and Validation Final Reports.
  • A Validation Plan defines the validation approach, activities, responsibilities, procedures, and requirements for the validation of a system or an item.
  • All test equipment used in the PQ was properly calibrated before use in the test. Copies of calibration certificates are attached to an appendix.
  • If the system acceptance criteria places limits on the number of critical, major, or minor defects that are permissible (e.g., none), the numbers permitted for one OQ protocol can be equal to or fewer than the numbers allowed for the entire system.

It Provides information on:

  • Responsibilities
    • Project Team
    • System Owners are responsible for
    • Quality Assurance (QA) is responsible for
  • Method
    • Life cycle approach
    • Conceptualize
    • Select Vendors and Systems
  • Quality Records
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