The Quality Assurance Reporting is a customizable tool offered by yudoo, for helping pharmaceutical companies to digitalize quality processes. It is possible to create multiple QA Report templates where to put selected parameters, like GMP alarms, Audit Trail exceptions, QA-Relevant Errors, Reconciliation formulas, Critical Parameters modifications and so on.
Collection of QA productivity metrics
Template-based reports
Suggestion of effective QA best practices
QA process issues detection
More information for QA team
Relevant information leads to actions
Easy-to-read visual reports greatly enhance data interpretation and decision-making processes, improving the reliability of QA procedures.
Lessons Learned from the past
Historical reporting makes it easier to identify defects in the QA process to be able to prevent mistakes before they happen again, as well as to improve the removal of QA issues that could stop the batch release.
Recommendations and improvements
It’s possible to integrate any information to be used for QA process improvement.
Features and compliance
The quality assurance system is specifically designed for the pharmaceutical market, and it is compliant with the industry regulations, with user access regulated by FDA 21 CFR part 11 and annex 11. All events are registered by the software in an audit trail file to keep track of all the security-relevant activities.
The continuous Software development follows Gamp 5, to always improve products quality and consistency.
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SEA Vision provides an extensive product portfolio of natively integrated solutions. Vision, traceability and data management solutions for pharmaceutical packaging lines are developed with a common approach to obtain a seamless ecosystem.