Quality Module
See every compliance event – inspections, recalls, sanctions and import alerts – from across the globe in one view, mapped to the sites and suppliers you depend on, so you spot what is coming before it reaches you.
Stop chasing scattered quality signals. Here’s how QYOBO works.
Inspection records in one portal, recalls in another, warning letters somewhere else, none of it tied to the suppliers you buy from. The QYOBO Quality module brings every signal into one place and tells you what is changing.
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Inspections, quality sanctions, recalls, import alerts – the compliance events that used to sit across a dozen separate portals now arrive in a single view. More than 100k inspection records across more than 24k m. sites today, each one tied to the site, product and company it concern. Optionally enriched with your internal audit data and seamlessly integrated.
QYOBO reads across thousands of inspections to surface which observations are new and which are trending more often than they used to, and flags where an FDA Warning Letter is most likely to land next. Agentic workflows turn that intelligence into action, automatically detecting repeat observations across audits and turning risk into an audit schedule – work that used to cost a quality team weeks now runs in the background.
More than 1,700 investigator profiles show who is active, what they inspect, where, and which quality systems they focus on. You know where a given inspector tends to dig before they walk in.
Benefits
BENEFITS: WALK INTO YOUR NEXT INSPECTION ALREADY KNOWING THE PATTERN
Global inspections, recalls and sanctions from more than a dozen countries land in one place, filtered to your manufacturing base. The warning sign that could have prevented a major quality event is no longer buried in a portal you never opened.
QYOBO processes 300+ regulatory databases and public company announcements continuously – the kind of coverage you could never assemble by checking portals yourself – and maps every item to the right asset: which products a site makes, which markets it serves, and which companies depend on it. Every alert arrives with the full picture attached.
If a supplier hits a problem at a site you do not even buy from, QYOBO detects it within hours and flags the potential GMP (Good Manufacturing Practice) risk, so you can act before it spreads to the site you rely on.
Agentic workflows make compliance continuous rather than periodic. Automatic detection of repeat observations after an audit alone saves a quality team weeks of work.
Across thousands of inspections, QYOBO identifies which observations are new and which are trending upward, tailored to the sites you run: finished dosage form (FDF) or active pharmaceutical ingredient (API), sterile or non-sterile, and by country.
Investigator profiles turn an unknown inspector into a known quantity, so you know where to double-check for the most common pitfalls before your next inspection.
More capabilities
One Platform. From Insight to Action.
See how QYOBO transforms pharma decision-making with AI-driven insights.
Questions?
Answers to your questions on how the Quality module drives better pharma decisions.
Inspections, quality sanctions, recalls and import alerts, drawn from 300+ regulatory databases worldwide plus public company announcements. Every record is mapped to the site, product and company it concerns.
It analyses trends across thousands of inspections to surface which observations are rising and where risk is concentrating, then highlights the sites most likely to draw an FDA Warning Letter next.
Yes. Filter to your manufacturing base and the kind of sites you run – FDF or API, sterile or non-sterile, by country – so you see only the signals that affect you.
Whether the investigator is active, their experience, total inspections, top inspected countries, auditing bodies, and their geographic and quality-system focus.
