QC eApprove

"With QC eApprove, we were able to meet all of the 21 CFR Part 11 requirements and customize the design to meet our existing internal procedures. This provided a significant savings in both time and costs."
- Richard Bodnar, Bayer

Use HP Quality Center in Validated Environments

QC eApprove provides controlled workflow and electronic signatures required to enable use of HP Quality Center in regulated environments and allow compliance with 21 CFR Part 11.

Avnet Services-HP Practice developed eApprove through core functionality found in HP Quality Center to assure that your eApprove implementation will survive as HP Quality Center evolves. With eApprove, companies can provide electronic signatures to approve requirements, tests, test sets, runs, and defects. The related workflow can be configured to match your process.

To reduce costs and shorten validation of QC eApprove and HP Quality Center, our HP Practice offers a customizable validation documentation suite that includes:

• Validation Plan
• Functional Requirements Specification (FRS)
• Design and Configuration Specification (DCS)
• Installation Qualification (IQ) / Configuration Verification
• Operational Qualification (OQ) / Functional Verification
• Performance Qualification (PQ) / Requirements Verification
• Risk Assessment
• Traceability Matrix
• Validation Summary Report

For more information, please contact us.

Rules Engine

QC eApprove's Rules Engine allows the electronic approval workflow process to be securely configured with a straightforward graphical user interface.

System Requirements

Software: HP Quality Center 8.2 SP1, 9.0, 9.2, 10, and 11 (including ALM)

Hardware & Operating System: Any system that meets HP Quality Center requirements