Because qualified UV/Vis platforms require strict change control, pharma and biopharma labs routinely run separate instruments for compliance and research. Protecting the audit trail is non-negotiable, but maintaining two systems for the same spectroscopy is an expensive workaround.
This compendium covers three distinct UV/Vis applications—formal instrument qualification, RNA purity assessment, and protein thermal characterization—all handled within the same UVWinLab environment, with procedural detail and application data for each.
Download the compendium to:
- Review the complete Operational Qualification (OQ) protocol and pass/fail results across all five pharmacopoeia parameters, including how the encrypted report is generated and certified
- Assess how the software automates RNA purity ratios and flags results against established thresholds
- Examine protein unfolding and refolding traces across a controlled thermal ramp, captured at differential rates through the transition zone
