The UOQ program provides, where applicable, pharmacopeial (USP, EP and JP) compliance with a design and approach that streamlines documentation across all major models of laboratory instruments, regardless of manufacturer.
Review Protocol – User-configurable for all set points and limits, offering customers full customization. The Review Protocol may be used for individual instruments or as a single protocol to harmonize all of your instruments.
Instrument Testing – Service engineers perform the qualification testing according to your specifications. Multiple systems can be tested at the same time and even overnight, significantly increasing uptime.
UOQ Report – An ultra-secure qualification report is generated using built-in calculations and pass/fail determinations for reliable documentation
Compliant – UOQ meets the highest regulatory standards and current international guidelines
Simplified – Easy-to-read reports with no hidden algorithms
Audit ready – Digital archiving of data and records makes gathering information easy for audits
UOQ is an innovative, harmonized, cross-platform approach that simplifies the entire qualification process. We offer the UOQ for GC, LC, IR and UV instruments.
Universal Operational Qualification
- Simplified approach to automated OQ with uniform reports across all instruments and technologies
- Uses existing data acquisition system, eliminating the need to validate an additional software platform
- Faster than comparable automated and traditional paper-based systems, resulting in significant increased instrument uptime and improved scientific productivity
- Reports are secure using digital certificate technology for encryption to prevent duplication and tampering